MEGAVISION CPX, MEGAVISION FA, MODEL I AND II— 510(k) K002920
Substantially EquivalentEscalon Medical Corp.
FDA 510(k) clearance K002920 for MEGAVISION CPX, MEGAVISION FA, MODEL I AND II, Substantially Equivalent on 2000-12-18. Applicant: Escalon Medical Corp.. Device class: 2.
Clearance details
- Applicant
- Escalon Medical Corp.
- Product code
- Code HKI
- Device class
- Class 2
- Regulation
- 21 CFR 886.1120
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New Berlin, WI, US
Recent devices under product code HKI
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