Piccolo Medical, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3038181770
- Devices
- 10
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
PM2™ System with ECGuide™ Connector Ref K252792
Regimes: 510(k) Registry: 510(k)PM2 System and ECGuide Connector Ref K240486
Regimes: 510(k) Registry: 510(k)PM2+ System and SmartPICC Stylet Ref K243484
Regimes: 510(k) Registry: 510(k)Piccolo Medical SmartPICC System Ref K200037
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3038181770
- Address
- 218 Mississippi St, San Francisco, CA, 94107
Frequently asked questions
How many devices does PICCOLO MEDICAL, INC. have in the registry?
The registry currently lists 10 devices for PICCOLO MEDICAL, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list PICCOLO MEDICAL, INC.'s devices?
Among its 10 most recently registered devices, PICCOLO MEDICAL, INC. has devices listed in FDA 510(k) (4 devices) and FDA GUDID (6 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do PICCOLO MEDICAL, INC.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for PICCOLO MEDICAL, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from PICCOLO MEDICAL, INC. in the registry?
The most recently registered devices listed for PICCOLO MEDICAL, INC. include Piccolo Medical FGS-15-773, Piccolo Medical FGN-15-634, Piccolo Medical FGN-15-779 and Piccolo Medical FGS-15-640.