510(k) K002920
K002920 is an FDA 510(k) premarket notification submitted by Escalon Medical Corp. for the device "MEGAVISION CPX, MEGAVISION FA, MODEL I AND II". The FDA issued a decision of Substantially Equivalent on Dec 18, 2000. The device falls under product code HKI (Camera, Ophthalmic, Ac-Powered), a Class II device regulated under 21 CFR 886.1120. Escalon Medical Corp. has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 18, 2000
- Date Received
- Sep 19, 2000
- 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
- 510(k)