Data / Medical devices / Calculator, Pulmonary Function Data
Calculator, Pulmonary Function Data (BZC): 22 FDA-registered makers in 9 countries
22 establishments in 9 countries are registered with the FDA to make Calculator, Pulmonary Function Data (product code BZC, Class 2, 21 CFR 868.1880). 13 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 90 510(k) clearances under this code, the latest on September 17, 2024, and lists 3 recall events (1 Class I). FDA data exported November 2, 2026.
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- Product code
- BZC
- Device class
- 2
- Regulation
- 868.1880
- Medical specialty
- Anesthesiology
Makers by country
| Country | Makers |
|---|---|
| United States | 10 |
| Germany | 4 |
| Israel | 2 |
| Italy | 1 |
| United Kingdom | 1 |
| Belgium | 1 |
| China | 1 |
| Poland | 1 |
| Mexico | 1 |
Makers of Calculator, Pulmonary Function Data
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Jaeger Medical GmbH | HOECHBERG Bavaria, Germany | Complaint file establishment, Manufacturer, Specification developer | 10 | August 23, 2019 | 0 | 1 | 1 | api.fda.gov |
| Cosmed S.R.L. | Albano Laziale, Roma, Italy | Exporter to the US, Manufacturer | 2 | June 20, 2017 | 0 | 0 | 0 | api.fda.gov |
| Coopersurgical, Inc. | Trumbull, CT, United States | Manufacturer | 1 | April 23, 1996 | 0 | 0 | 0 | api.fda.gov |
| Cortex Biophysik GMBH | LEIPZIG Saxony, Germany | Manufacturer | 1 | February 22, 2001 | 0 | 0 | 0 | api.fda.gov |
| Jones Medical Instrument Co. | Oak Brook, IL, United States | Manufacturer | 1 | August 20, 1981 | 0 | 0 | 0 | api.fda.gov |
| KoKo PFT LTD. | Waltham Abbey Essex, United Kingdom | Manufacturer | 1 | December 22, 2005 | 0 | 0 | 0 | api.fda.gov |
| Medisoft S.A. | DINANT Namur, Belgium | Manufacturer | 1 | December 9, 1996 | 0 | 0 | 0 | api.fda.gov |
| Pulmone Advanced Medical Devices, Ltd. | Raananna Central, Israel | Manufacturer | 1 | October 21, 2016 | 0 | 0 | 0 | api.fda.gov |
| Pulmone Usa Inc | Carrollton, TX, United States | Specification developer | 1 | October 21, 2016 | 0 | 0 | 0 | api.fda.gov |
| Parvo Medics Inc. | Murray, UT, United States | Manufacturer | 1 | June 16, 1995 | 0 | 0 | 0 | api.fda.gov |
| Respironics Inc. | Murrysville, PA, United States | Complaint file establishment, Specification developer | 1 | January 22, 1997 | 0 | 0 | 0 | api.fda.gov |
| Technopulm, Ltd. | Petah Tikva Central, Israel | Manufacturer | 1 | September 17, 2024 | 0 | 0 | 0 | api.fda.gov |
| Vacumed, Div. Of Vacumetrics, Inc. | Ventura, CA, United States | Manufacturer | 1 | April 2, 1986 | 0 | 0 | 0 | api.fda.gov |
| Amphenol Medical Technologies (Dongguan) Co., Ltd. | Dongguan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kimball Electronics Poland Sp.z o.o | Tarnowo Podgorne Wielkopolskie, Poland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Graphics Corp. | Saint Paul, MN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Minnetronix, Inc. | Saint Paul, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Productos Urologos De Mexico S.A. De C.V. | MEXICALI Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pulsion Medical Systems Se | Aschheim, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips Medizin Systeme Boeblingen GmbH | BOEBLINGEN Baden-Wurttemberg, Germany | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips North America LLC | Murrysville, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips North America LLC | Export, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated September 17, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.