STS RANGE , MODELS STS20,STS30,STS40— 510(k) K012008

Name: FDA 510(k) clearance K012008
Creator: U.S. Food and Drug Administration
Published: 2001-09-21

Substantially Equivalent

Huntleigh Healthcare, Inc.

FDA 510(k) clearance K012008 for STS RANGE , MODELS STS20,STS30,STS40, Substantially Equivalent on 2001-09-21. Applicant: Huntleigh Healthcare, Inc.. Device class: 2.

Clearance details

Applicant: Huntleigh Healthcare, Inc.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2001-06-27
Decision date: 2001-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eatontown, NJ, US

Download summary PDF View on FDA.gov ↗

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