510(k) K873388
K873388 is an FDA 510(k) premarket notification submitted by Keeler Instruments, Inc. for the device "KEELER CTU CRYO SYSTEM". The FDA issued a decision of Substantially Equivalent on November 13, 1987. The device falls under product code HPS (Unit, Cryophthalmic), a Class II device regulated under 21 CFR 886.4170. Keeler Instruments, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 13, 1987
- Date Received
- August 24, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Unit, Cryophthalmic
- Device Class
- Class II
- Regulation Number
- 886.4170
- Review Panel
- OP
- Submission Type