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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

CountryMakers
United States10
Germany4
Israel2
Italy1
United Kingdom1
Belgium1
China1
Poland1
Mexico1

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.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Jaeger Medical GmbHHOECHBERG Bavaria, GermanyComplaint file establishment, Manufacturer, Specification developer10August 23, 2019011api.fda.gov
Cosmed S.R.L.Albano Laziale, Roma, ItalyExporter to the US, Manufacturer2June 20, 2017000api.fda.gov
Coopersurgical, Inc.Trumbull, CT, United StatesManufacturer1April 23, 1996000api.fda.gov
Cortex Biophysik GMBHLEIPZIG Saxony, GermanyManufacturer1February 22, 2001000api.fda.gov
Jones Medical Instrument Co.Oak Brook, IL, United StatesManufacturer1August 20, 1981000api.fda.gov
KoKo PFT LTD.Waltham Abbey Essex, United KingdomManufacturer1December 22, 2005000api.fda.gov
Medisoft S.A.DINANT Namur, BelgiumManufacturer1December 9, 1996000api.fda.gov
Pulmone Advanced Medical Devices, Ltd.Raananna Central, IsraelManufacturer1October 21, 2016000api.fda.gov
Pulmone Usa IncCarrollton, TX, United StatesSpecification developer1October 21, 2016000api.fda.gov
Parvo Medics Inc.Murray, UT, United StatesManufacturer1June 16, 1995000api.fda.gov
Respironics Inc.Murrysville, PA, United StatesComplaint file establishment, Specification developer1January 22, 1997000api.fda.gov
Technopulm, Ltd.Petah Tikva Central, IsraelManufacturer1September 17, 2024000api.fda.gov
Vacumed, Div. Of Vacumetrics, Inc.Ventura, CA, United StatesManufacturer1April 2, 1986000api.fda.gov
Amphenol Medical Technologies (Dongguan) Co., Ltd.Dongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Kimball Electronics Poland Sp.z o.oTarnowo Podgorne Wielkopolskie, PolandContract manufacturer0000api.fda.gov
Medical Graphics Corp.Saint Paul, MN, United StatesManufacturer0000api.fda.gov
Minnetronix, Inc.Saint Paul, MN, United StatesContract manufacturer0000api.fda.gov
Productos Urologos De Mexico S.A. De C.V.MEXICALI Baja California, MexicoContract manufacturer0000api.fda.gov
Pulsion Medical Systems SeAschheim, GermanyContract manufacturer0000api.fda.gov
Philips Medizin Systeme Boeblingen GmbHBOEBLINGEN Baden-Wurttemberg, GermanyComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Philips North America LLCMurrysville, PA, United StatesContract manufacturer0000api.fda.gov
Philips North America LLCExport, PA, United StatesContract manufacturer0000api.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.