F.L.W. Plastics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What F.L.W. Plastics, Inc. makes
F.L.W. Plastics, Inc. manufactures manual disposable pulmonary resuscitators, anesthesia breathing circuits, mass spectrometry monitoring lines and connectors, and bacterial and viral filters.
These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Manual Disposable Pulmonary Resuscitator Ref K895169
510(k) 510(k)Anethesia Breathing Circuit Ref K895357
510(k) 510(k)- 510(k) 510(k)
Bacterial And Viral Filter Ref K895233
510(k) 510(k)
Frequently asked questions
How many devices does F.L.W. Plastics, Inc. have in the registry?
The registry currently lists 4 devices for F.L.W. Plastics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list F.L.W. Plastics, Inc.'s devices?
Among its 4 most recently registered devices, F.L.W. Plastics, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do F.L.W. Plastics, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for F.L.W. Plastics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from F.L.W. Plastics, Inc. in the registry?
The most recently registered devices listed for F.L.W. Plastics, Inc. include MANUAL DISPOSABLE PULMONARY RESUSCITATOR, ANETHESIA BREATHING CIRCUIT, MASS SPECTROMETRY MONITORING LINES AND CONNECTORS and BACTERIAL AND VIRAL FILTER.