ELECTRIC WIRE DRIVER, MODEL 2640E— 510(k) K930205

Name: FDA 510(k) clearance K930205
Creator: U.S. Food and Drug Administration
Published: 1993-08-02

Substantially Equivalent

Micro Surgical Instruments Corp.

FDA 510(k) clearance K930205 for ELECTRIC WIRE DRIVER, MODEL 2640E, Substantially Equivalent on 1993-08-02. Applicant: Micro Surgical Instruments Corp.. Device class: 1.

Clearance details

Applicant: Micro Surgical Instruments Corp.
Product code: Code HXJ
Device class: Class 1
Regulation: 21 CFR 888.4540
Advisory panel: Orthopedic
Date received: 1993-01-15
Decision date: 1993-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valencia, CA, US

Download summary PDF View on FDA.gov ↗

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