Pm America, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Pm America, Inc. makes
Pm America, Inc. manufactures medical devices including the POLI-MAK MODEL F-4, AUTO PREP, DSD, MODEL 4900 OFF-LINE PREPARATION SYSTEM, and POLI-MAK II, which are used for preparation and processing purposes.
The company's devices are all classified as Class I and are listed in the FDA 510(k) registry. Pm America, Inc. is based in the US.
Catalogue
Poli-Mak Model F-4 (Final Ref K820748
Regimes: 510(k) Registry: 510(k)Auto Prep Ref K830319
Regimes: 510(k) Registry: 510(k)Dsd Ref K812983
Regimes: 510(k) Registry: 510(k)Model 4900 Off-Line Preparation System Ref K801271
Regimes: 510(k) Registry: 510(k)Poli-Mak Ii Ref K813102
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pm America, Inc. have in the registry?
The registry currently lists 5 devices for Pm America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pm America, Inc.'s devices?
Among its 5 most recently registered devices, Pm America, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Pm America, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Pm America, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pm America, Inc. in the registry?
The most recently registered devices listed for Pm America, Inc. include POLI-MAK MODEL F-4 (FINAL, AUTO PREP, DSD and MODEL 4900 OFF-LINE PREPARATION SYSTEM.