KESTREL LENS CASE 1543-893S/P-1700-2611— 510(k) K900054

Substantially Equivalent

Kestrel

FDA 510(k) clearance K900054 for KESTREL LENS CASE 1543-893S/P-1700-2611, Substantially Equivalent on 1990-01-30. Applicant: Kestrel.

Clearance details

Applicant: Kestrel
Product code: Code LRX
Advisory panel: Ophthalmic
Date received: 1990-01-03
Decision date: 1990-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbus, IN, US

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