DIGITAL BEDSIDE SCALE #5000— 510(k) K830171

Name: FDA 510(k) clearance K830171
Creator: U.S. Food and Drug Administration
Published: 1983-02-18

Substantially Equivalent

Acme Medical Scale Co.

FDA 510(k) clearance K830171 for DIGITAL BEDSIDE SCALE #5000, Substantially Equivalent on 1983-02-18. Applicant: Acme Medical Scale Co.. Device class: 1.

Clearance details

Applicant: Acme Medical Scale Co.
Product code: Code FRW
Device class: Class 1
Regulation: 21 CFR 880.2720
Advisory panel: General Hospital
Date received: 1983-01-18
Decision date: 1983-02-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.