RYDER CONTACT LENS CASE MODEL 10670— 510(k) K951182

Name: FDA 510(k) clearance K951182
Creator: U.S. Food and Drug Administration
Published: 1995-05-16

Substantially Equivalent

Bradstreet Clinical Research Assoc., Inc.

FDA 510(k) clearance K951182 for RYDER CONTACT LENS CASE MODEL 10670, Substantially Equivalent on 1995-05-16. Applicant: Bradstreet Clinical Research Assoc., Inc.. Device class: 2.

Clearance details

Applicant: Bradstreet Clinical Research Assoc., Inc.
Product code: Code LRX
Device class: Class 2
Regulation: 21 CFR 886.5928
Advisory panel: Ophthalmic
Date received: 1995-03-16
Decision date: 1995-05-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brunswick, NJ, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.