BOSTON CONTACT LENS CASE— 510(k) K962512

Name: FDA 510(k) clearance K962512
Creator: U.S. Food and Drug Administration
Published: 1996-07-12

Substantially Equivalent

Polymer Technology Div. Wilmington Partners, L.P.

FDA 510(k) clearance K962512 for BOSTON CONTACT LENS CASE, Substantially Equivalent on 1996-07-12. Applicant: Polymer Technology Div. Wilmington Partners, L.P.. Device class: 2.

Clearance details

Applicant: Polymer Technology Div. Wilmington Partners, L.P.
Product code: Code LRX
Device class: Class 2
Regulation: 21 CFR 886.5928
Advisory panel: Ophthalmic
Date received: 1996-06-27
Decision date: 1996-07-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, 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.