K841718Unknown
Frekatheter Venous Catheterisation Sys
Fresenius USA, Inc., Walker MI / Traditional, Unknown
K841718 is the FDA 510(k) clearance record for FREKATHETER VENOUS CATHETERISATION SYS, cleared for Fresenius USA, Inc. on . FDA records list 38 510(k) clearances for Fresenius USA, Inc., from to . As of , FDA records show no recalls naming K841718.
Clearance record
- Decision date
- Received
- (0 days to decision)
- Review panel
- Unknown
- Applicant
- Fresenius USA, Inc. 4221 Richmond Rd., NW, Walker MI
- Third party review
- No
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