WELLS LAMONT CUT RESISTANT SURGICAL GLOVE LINERS— 510(k) K922407

Name: FDA 510(k) clearance K922407
Creator: U.S. Food and Drug Administration
Published: 1993-06-15

Substantially Equivalent

Wells Lamont Corp.

FDA 510(k) clearance K922407 for WELLS LAMONT CUT RESISTANT SURGICAL GLOVE LINERS, Substantially Equivalent on 1993-06-15. Applicant: Wells Lamont Corp.. Device class: 1.

Clearance details

Applicant: Wells Lamont Corp.
Product code: Code LYU
Device class: Class 1
Regulation: 21 CFR 878.4040
Advisory panel: General, Plastic Surgery
Date received: 1992-05-21
Decision date: 1993-06-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Niles, IL, US

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