510(k) K812706
K812706 is an FDA 510(k) premarket notification submitted by Mosebach Electric & Supply for the device "MILLER/NADLER GLARE TESTER". The FDA issued a decision of Substantially Equivalent on November 16, 1981. The device falls under product code HOS (Projector, Ophthalmic), a Class I device regulated under 21 CFR 886.1680.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 16, 1981
- Date Received
- September 24, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Projector, Ophthalmic
- Device Class
- Class I
- Regulation Number
- 886.1680
- Review Panel
- OP
- Submission Type