510(k) K823719
K823719 is an FDA 510(k) premarket notification submitted by Nikon, Inc. for the device "AML (ANGLE MAGNIFYING LENS". The FDA issued a decision of Substantially Equivalent on January 5, 1983. The device falls under product code HKI (Camera, Ophthalmic, Ac-Powered), a Class II device regulated under 21 CFR 886.1120. Nikon, Inc. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 5, 1983
- Date Received
- December 10, 1982
- 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