Berman, Pcp & Consultants, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
What Berman, Pcp & Consultants, Inc. makes
Berman, Pcp & Consultants, Inc. makes scalp vein sets, infusion sets (types S and J), blood collection sets (type H), blood administration sets (type R), and disposable syringes in 2 mL, 5 mL, and L0 mL sizes.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Scalp Vein Set Ref K771271
Regimes: 510(k) Registry: 510(k)Infusion Set Type S Ref K771267
Regimes: 510(k) Registry: 510(k)Scalp Vein Set Ref K771983
Regimes: 510(k) Registry: 510(k)Blood Collection Set Type H Ref K771269
Regimes: 510(k) Registry: 510(k)Infusion Set Type J Ref K771268
Regimes: 510(k) Registry: 510(k)Disp. Syringes: 2, 5 & L0 Mi. Ref K771272
Regimes: 510(k) Registry: 510(k)Blood Administration Type R Ref K771270
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Berman, Pcp & Consultants, Inc. have in the registry?
The registry currently lists 7 devices for Berman, Pcp & Consultants, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Berman, Pcp & Consultants, Inc.'s devices?
Among its 7 most recently registered devices, Berman, Pcp & Consultants, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Berman, Pcp & Consultants, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Berman, Pcp & Consultants, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Berman, Pcp & Consultants, Inc. in the registry?
The most recently registered devices listed for Berman, Pcp & Consultants, Inc. include SCALP VEIN SET, INFUSION SET TYPE S, BLOOD COLLECTION SET TYPE H and INFUSION SET TYPE J.