3M MAXI-DRIVER II DBATTERY POWERED SYSTEM— 510(k) K932307

Name: FDA 510(k) clearance K932307
Creator: U.S. Food and Drug Administration
Published: 1994-01-07

Substantially Equivalent

3M Health Care, Ltd.

FDA 510(k) clearance K932307 for 3M MAXI-DRIVER II DBATTERY POWERED SYSTEM, Substantially Equivalent on 1994-01-07. Applicant: 3M Health Care, Ltd.. Device class: 1.

Clearance details

Applicant: 3M Health Care, Ltd.
Product code: Code KIJ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1993-05-11
Decision date: 1994-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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