RYDER CONTACT LENS CASE— 510(k) K943921

Name: FDA 510(k) clearance K943921
Creator: U.S. Food and Drug Administration
Published: 1994-10-11

Substantially Equivalent

Clinical Research Assoc.

FDA 510(k) clearance K943921 for RYDER CONTACT LENS CASE, Substantially Equivalent on 1994-10-11. Applicant: Clinical Research Assoc.. Device class: 2.

Clearance details

Applicant: Clinical Research Assoc.
Product code: Code LRX
Device class: Class 2
Regulation: 21 CFR 886.5928
Advisory panel: Ophthalmic
Date received: 1994-08-12
Decision date: 1994-10-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brunswick, NJ, US

Download summary PDF View on FDA.gov ↗

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