K & G Healthcare Ind., Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What K & G Healthcare Ind., Inc. makes
K & G Healthcare Ind., Inc. manufactures disposable respiratory filters, including spirometer filters, viral-bacterial filters (e.g., the Nicholas II series), and vacuum suction filters designed for single-use in medical and clinical settings.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records in the U.S. The company is based in the United States.
Catalogue
Spirometer Filter Ref K812573
Regimes: 510(k) Registry: 510(k)Nicholas Ii, Viral-Bacterial Filter Ref K811546
Regimes: 510(k) Registry: 510(k)Vacuum Suction Filter Ref K812139
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does K & G Healthcare Ind., Inc. have in the registry?
The registry currently lists 3 devices for K & G Healthcare Ind., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list K & G Healthcare Ind., Inc.'s devices?
Among its 3 most recently registered devices, K & G Healthcare Ind., Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do K & G Healthcare Ind., Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for K & G Healthcare Ind., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from K & G Healthcare Ind., Inc. in the registry?
The most recently registered devices listed for K & G Healthcare Ind., Inc. include SPIROMETER FILTER, NICHOLAS II, VIRAL-BACTERIAL FILTER and VACUUM SUCTION FILTER.