DeviceClearance

MEGAVISION CPX, MEGAVISION FA, MODEL I AND II— 510(k) K002920

Substantially Equivalent

Escalon 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..

Clearance details

Applicant
Escalon Medical Corp.
Product code
Code HKI
Advisory panel
Ophthalmic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
New Berlin, WI, US
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