Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K832816Substantially Equivalent

Hall Arthrotome

American Sterilizer Co., Walker MI / Traditional, Substantially Equivalent

K832816 is the FDA 510(k) clearance record for HALL ARTHROTOME, cleared for American Sterilizer Co. on . FDA records list 36 510(k) clearances for American Sterilizer Co., from to . As of , FDA records show no recalls naming K832816.

Clearance record

Decision date
Received
(101 days to decision)
Review panel
Unknown
Applicant
American Sterilizer Co. 4221 Richmond Rd., NW, Walker MI
Third party review
No