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

Name: FDA 510(k) clearance K900054
Creator: U.S. Food and Drug Administration
Published: 1990-01-30

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. Device class: 2.

Clearance details

Applicant: Kestrel
Product code: Code LRX
Device class: Class 2
Regulation: 21 CFR 886.5928
Advisory panel: Ophthalmic
Date received: 1990-01-03
Decision date: 1990-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbus, IN, US

Download summary PDF View on FDA.gov ↗

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K901748 — KESTREL LENS CASE (208-12NT POLYSTYRENE)1990-05-31
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Data sourced from openFDA. This site is unofficial and independent of the FDA.