K840641 is the FDA 510(k) clearance record for VESSEL DILATOR, cleared for Aries Medical, Inc. on . FDA records list 19 510(k) clearances for Aries Medical, Inc., from to . As of , FDA records show no recalls naming K840641.
Clearance record
- Decision date
- Received
- (0 days to decision)
- Review panel
- Unknown
- Applicant
- Aries Medical, Inc. 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.