Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K790886Substantially Equivalent

Corrugated Flexible Polyethylene

Airlife, Inc., Mchenry IL / Traditional, Substantially Equivalent

K790886 is the FDA 510(k) clearance record for CORRUGATED FLEXIBLE POLYETHYLENE, cleared for Airlife, Inc. on . FDA records list 76 510(k) clearances for Airlife, Inc., from to . As of , FDA records show no recalls naming K790886.

Clearance record

Decision date
Received
(10 days to decision)
Review panel
Unknown
Applicant
Airlife, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No