Data / Medical devices / Gas, Collecting Vessel
Gas, Collecting Vessel (KGK): 9 FDA-registered makers in 6 countries
9 establishments in 6 countries are registered with the FDA to make Gas, Collecting Vessel (product code KGK, Class 1, 21 CFR 868.1575). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on October 15, 1986, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- KGK
- Device class
- 1
- Regulation
- 868.1575
- Medical specialty
- Anesthesiology
Makers by country
| Country | Makers |
|---|---|
| China | 2 |
| Japan | 2 |
| United Kingdom | 2 |
| Taiwan | 1 |
| United States | 1 |
| Israel | 1 |
Makers of Gas, Collecting Vessel
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 |
|---|---|---|---|---|---|---|---|---|
| Galemed Corp. | WU-JIA Yilan, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GaleMed (Xiamen) Co., Ltd. | XIAMEN Fujian, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hubei V-Medical Products Co., Ltd. | Xiantao Hubei, China | Contract manufacturer, Exporter to the US | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nihon Kohden Corp. | SHINJUKU-KU Tokyo, Japan | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nihon Kohden Corporation - Tokorozawa establishment Advanced Technology Center | Tokorozawa Saitama, Japan | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pulmobiomed Ltd. | Newcastle upon Tyne, United Kingdom | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Respiratory Research, Inc. | Austin, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shahak-Tec Ltd. | Zichron Yaakov Haifa, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Spiracheck Limited | NORTHWOOD Hillingdon, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated October 15, 1986. 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.