HAND DRILL, MODEL 11-9901-7— 510(k) K022712

Name: FDA 510(k) clearance K022712
Creator: U.S. Food and Drug Administration
Published: 2002-11-12

Substantially Equivalent

Medical Design, LLC

FDA 510(k) clearance K022712 for HAND DRILL, MODEL 11-9901-7, Substantially Equivalent on 2002-11-12. Applicant: Medical Design, LLC. Device class: 2.

Clearance details

Applicant: Medical Design, LLC
Product code: Code HBG
Device class: Class 2
Regulation: 21 CFR 882.4300
Advisory panel: Neurology
Date received: 2002-08-14
Decision date: 2002-11-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brandon, SD, US

Download summary PDF View on FDA.gov ↗

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