510(k) K934663
K934663 is an FDA 510(k) premarket notification submitted by Canon USA, Inc. for the device "60 DEGREE FUNDUS CAMERA, CF-60UD". The FDA issued a decision of Substantially Equivalent on February 22, 1994. The device falls under product code HKI (Camera, Ophthalmic, Ac-Powered), a Class II device regulated under 21 CFR 886.1120. Canon USA, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 22, 1994
- Date Received
- September 28, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Camera, Ophthalmic, Ac-Powered
- Device Class
- Class II
- Regulation Number
- 886.1120
- Review Panel
- OP
- Submission Type