Pierrel Pharma S.r.l.
ItalyFDA applicant, unverified
- Devices
- 1
What Pierrel Pharma S.r.l. makes
Pierrel Pharma S.R.L. makes G.o.c.c.l.e.s.
The device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
G.o.c.c.l.e.s. Ref K151630
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pierrel Pharma S.R.L. have in the registry?
The registry currently lists 1 device for Pierrel Pharma S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pierrel Pharma S.R.L.'s devices?
Among its 1 most recently registered device, Pierrel Pharma S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Pierrel Pharma S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pierrel Pharma S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pierrel Pharma S.R.L. in the registry?
The most recently registered devices listed for Pierrel Pharma S.R.L. include G.o.c.c.l.e.s..