K841793Substantially Equivalent
Cooper Lasersonics Nd:yag Laser 8000
Cooper Lasersonics, Inc., Mchenry IL / Traditional, Substantially Equivalent
K841793 is the FDA 510(k) clearance record for COOPER LASERSONICS ND:YAG LASER 8000, cleared for Cooper Lasersonics, Inc. on . FDA records list 54 510(k) clearances for Cooper Lasersonics, Inc., from to . As of , FDA records show no recalls naming K841793.
Clearance record
- Decision date
- Received
- (38 days to decision)
- Review panel
- Unknown
- Applicant
- Cooper Lasersonics, 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.
