K822849Substantially Equivalent
Raaf Dual Lumen Catheter
Quinton, Inc., Walker MI / Traditional, Substantially Equivalent
K822849 is the FDA 510(k) clearance record for RAAF DUAL LUMEN CATHETER, cleared for Quinton, Inc. on . FDA records list 164 510(k) clearances for Quinton, Inc., from to . As of , FDA records show no recalls naming K822849.
Clearance record
- Decision date
- Received
- (67 days to decision)
- Review panel
- Unknown
- Applicant
- Quinton, Inc. 4221 Richmond Rd., NW, Walker MI
- Third party review
- No
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