SURGICAL SPEARS— 510(k) K923922

Name: FDA 510(k) clearance K923922
Creator: U.S. Food and Drug Administration
Published: 1993-03-19

Substantially Equivalent

Ultracell Medical Technologies, Inc.

FDA 510(k) clearance K923922 for SURGICAL SPEARS, Substantially Equivalent on 1993-03-19. Applicant: Ultracell Medical Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Ultracell Medical Technologies, Inc.
Product code: Code HOZ
Device class: Class 2
Regulation: 21 CFR 886.4790
Advisory panel: Ophthalmic
Date received: 1992-08-05
Decision date: 1993-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Stonington, CT, US

Download summary PDF View on FDA.gov ↗

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