510(k) K062412
K062412 is an FDA 510(k) premarket notification submitted by Keeler Instruments, Inc. for the device "CRYOMATIC". The FDA issued a decision of Substantially Equivalent on November 6, 2006. The device falls under product code HRN (Unit, Cryophthalmic, Ac-Powered), 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 6, 2006
- Date Received
- August 17, 2006
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Unit, Cryophthalmic, Ac-Powered
- Device Class
- Class II
- Regulation Number
- 886.4170
- Review Panel
- OP
- Submission Type