DONWAY LIFTING FRAME— 510(k) K851660

Name: FDA 510(k) clearance K851660
Creator: U.S. Food and Drug Administration
Published: 1985-08-07

Substantially Equivalent

Australian Biomedical Corporation , Ltd.

FDA 510(k) clearance K851660 for DONWAY LIFTING FRAME, Substantially Equivalent on 1985-08-07. Applicant: Australian Biomedical Corporation , Ltd.. Device class: 1.

Clearance details

Applicant: Australian Biomedical Corporation , Ltd.
Product code: Code FPP
Device class: Class 1
Regulation: 21 CFR 880.6900
Advisory panel: General Hospital
Date received: 1985-04-23
Decision date: 1985-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Australia, AU

Download summary PDF View on FDA.gov ↗

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