SPATULA'S #'S 7618,7248,7240,7242,5108— 510(k) K791983

Name: FDA 510(k) clearance K791983
Creator: U.S. Food and Drug Administration
Published: 1979-10-04

Substantially Equivalent

Edward Weck, Inc.

FDA 510(k) clearance K791983 for SPATULA'S #'S 7618,7248,7240,7242,5108, Substantially Equivalent on 1979-10-04. Applicant: Edward Weck, Inc.. Device class: 1.

Clearance details

Applicant: Edward Weck, Inc.
Product code: Code HND
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1979-09-25
Decision date: 1979-10-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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