Chestnut Medical Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Alligator Retrieval Device (Ard) Ref K043580
Regimes: 510(k) Registry: 510(k)Marksmann Catheter Ref K091559
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Chestnut Medical Technologies, Inc. have in the registry?
The registry currently lists 3 devices for Chestnut Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Chestnut Medical Technologies, Inc.'s devices?
Among its 3 most recently registered devices, Chestnut Medical Technologies, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Chestnut Medical Technologies, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Chestnut Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Chestnut Medical Technologies, Inc. in the registry?
The most recently registered devices listed for Chestnut Medical Technologies, Inc. include ALLIGATOR RETRIEVAL DEVICE (ARD), MARKSMANN CATHETER and ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX.