510(k) K833387
K833387 is an FDA 510(k) premarket notification submitted by Cooper Medical Corp. for the device "ARGON LASER SURGICAL SYSTEM 770". The FDA issued a decision of Substantially Equivalent on April 18, 1984. Cooper Medical Corp. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 18, 1984
- Date Received
- September 29, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No