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
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
