510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K842781Unknown

Permalid Pak

CooperVision, Inc., Southampton, GB / Traditional, Unknown
FDA source (opens on fda.gov)

K842781 is the FDA 510(k) clearance record for PERMALID PAK, cleared for CooperVision, Inc. on . FDA records list 97 510(k) clearances for CooperVision, Inc., from to . As of , FDA records show no recalls naming K842781.

Clearance record

Decision date
Received
(381 days to decision)
Review panel
Unknown
Applicant
CooperVision, Inc. Permalens House, Southampton, GB
Third party review
No