510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K863551Substantially Equivalent

Modified Medi-Quet Tourniquet, Model #2740-00

Depuy, Inc., Warsaw IN / Traditional, Substantially Equivalent

K863551 is the FDA 510(k) clearance record for MODIFIED MEDI-QUET TOURNIQUET, MODEL #2740-00, cleared for Depuy, Inc. on . FDA records list 220 510(k) clearances for Depuy, Inc., from to . As of , FDA records show no recalls naming K863551.

Clearance record

Decision date
Received
(21 days to decision)
Review panel
Unknown
Applicant
Depuy, Inc. P.O. Box 988, Warsaw IN
Third party review
No