Avocet Medical, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What Avocet Medical, Inc. makes
Avocet Medical, Inc. manufactures the AVOCET ACUSURE and AVOCET ACUSURE PRO devices for patient self-testing and professional use, respectively, along with the AVOCET SYSTEM LIQUID CONTROL LEVEL 1 and LEVEL 2, and the AVOCET PT system.
The company's products are Class II devices listed in the FDA 510(k) registry, and Avocet Medical is based in the US.
Catalogue
- 510(k) 510(k)
Avocet System Liquid Control Level 1 And Level 2 Ref K980982
510(k) 510(k)Avocet Acusure System Ref K991286
510(k) 510(k)Avocet Pt Ref K980839
510(k) 510(k)
Frequently asked questions
How many devices does Avocet Medical, Inc. have in the registry?
The registry currently lists 4 devices for Avocet Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Avocet Medical, Inc.'s devices?
Among its 4 most recently registered devices, Avocet Medical, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Avocet Medical, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Avocet Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Avocet Medical, Inc. in the registry?
The most recently registered devices listed for Avocet Medical, Inc. include AVOCET ACUSURE (FOR PATIENT SELF-TESTING) AND AVOCET ACUSURE PRO (FOR PROFESSIONAL USE), AVOCET SYSTEM LIQUID CONTROL LEVEL 1 AND LEVEL 2, AVOCET ACUSURE SYSTEM and AVOCET PT.