ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADE— 510(k) K884862

Name: FDA 510(k) clearance K884862
Creator: U.S. Food and Drug Administration
Published: 1988-12-27

Substantially Equivalent

Anchor Products Co.

FDA 510(k) clearance K884862 for ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADE, Substantially Equivalent on 1988-12-27. Applicant: Anchor Products Co.. Device class: 1.

Clearance details

Applicant: Anchor Products Co.
Product code: Code GES
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1988-11-21
Decision date: 1988-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Addison, IL, US

Download summary PDF View on FDA.gov ↗

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