COLORADO NEEDLE ELECTRODE— 510(k) K881763

Name: FDA 510(k) clearance K881763
Creator: U.S. Food and Drug Administration
Published: 1988-06-20

Substantially Equivalent

Colorado Biomedical, Inc.

FDA 510(k) clearance K881763 for COLORADO NEEDLE ELECTRODE, Substantially Equivalent on 1988-06-20. Applicant: Colorado Biomedical, Inc.. Device class: 2.

Clearance details

Applicant: Colorado Biomedical, Inc.
Product code: Code JOS
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 1988-04-25
Decision date: 1988-06-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Evergreen, CO, US

Download summary PDF View on FDA.gov ↗

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