ARTHROBOT(TM) 75 (190 CM) GENERAL PURPOSE DRAPE— 510(k) K911520

Name: FDA 510(k) clearance K911520
Creator: U.S. Food and Drug Administration
Published: 1991-08-02

Substantially Equivalent

Andronic Devices, Ltd.

FDA 510(k) clearance K911520 for ARTHROBOT(TM) 75 (190 CM) GENERAL PURPOSE DRAPE, Substantially Equivalent on 1991-08-02. Applicant: Andronic Devices, Ltd.. Device class: 2.

Clearance details

Applicant: Andronic Devices, Ltd.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1991-04-04
Decision date: 1991-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richmond,B.C. V6v-2j2, CA

Download summary PDF View on FDA.gov ↗

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