K863336Substantially Equivalent
Cordipak Angiography Tray
Angi-Pak Corp., Miami FL / Traditional, Substantially Equivalent
K863336 is the FDA 510(k) clearance record for CORDIPAK ANGIOGRAPHY TRAY, cleared for Angi-Pak Corp. on . FDA records list 2 510(k) clearances for Angi-Pak Corp., from to . As of , FDA records show no recalls naming K863336.
Clearance record
- Decision date
- Received
- (15 days to decision)
- Review panel
- Unknown
- Applicant
- Angi-Pak Corp. 13780 SW 73 Ct., Miami FL
- Third party review
- No
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