Gallini Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 7
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pan (Chiba Aspirating Needle) Ref K970872
Regimes: 510(k) Registry: 510(k)Tz Ref K964777
Regimes: 510(k) Registry: 510(k)Speed-Cut Ref K961407
Regimes: 510(k) Registry: 510(k)Biomid Bone Marrow Biopsy Needle Ref K962569
Regimes: 510(k) Registry: 510(k)Acri Iliac Crest Aspiration Biopsy Needles Ref K962568
Regimes: 510(k) Registry: 510(k)Isan Sternal-Iliac Aspiration Biopsy Needle Ref K962570
Regimes: 510(k) Registry: 510(k)Tr Needle Ref K970871
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gallini Intl., Inc. have in the registry?
The registry currently lists 7 devices for Gallini Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gallini Intl., Inc.'s devices?
Among its 7 most recently registered devices, Gallini Intl., Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Gallini Intl., Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Gallini Intl., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gallini Intl., Inc. in the registry?
The most recently registered devices listed for Gallini Intl., Inc. include PAN (CHIBA ASPIRATING NEEDLE), TZ, SPEED-CUT and BIOMID BONE MARROW BIOPSY NEEDLE.