Patton Medical Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Patton Medical Corp. makes
Patton Medical Corp. makes the Patton Endo-Bag, Patton Speculum, Funnel Trocar, and Patton Tripol devices.
These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Patton Endo-Bag Ref K012150
Regimes: 510(k) Registry: 510(k)Patton Speculum Ref K991963
Regimes: 510(k) Registry: 510(k)Funnel Trocar Ref K992324
Regimes: 510(k) Registry: 510(k)Patton Tripol Ref K012279
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Patton Medical Corp. have in the registry?
The registry currently lists 4 devices for Patton Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Patton Medical Corp.'s devices?
Among its 4 most recently registered devices, Patton Medical Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Patton Medical Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Patton Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Patton Medical Corp. in the registry?
The most recently registered devices listed for Patton Medical Corp. include PATTON ENDO-BAG, PATTON SPECULUM, FUNNEL TROCAR and PATTON TRIPOL.