K790352 is the FDA 510(k) clearance record for NEPHROSS 11F100, cleared for Redy Laboratories on . FDA records list 2 510(k) clearances for Redy Laboratories, from to . As of , FDA records show no recalls naming K790352.
Clearance record
- Decision date
- Received
- (0 days to decision)
- Review panel
- Unknown
- Applicant
- Redy Laboratories 803 N. Front St. Suite 3, Mchenry IL
- 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.
