90DX MULTITEST METER, MODIFICATION— 510(k) K925210

Name: FDA 510(k) clearance K925210
Creator: U.S. Food and Drug Administration
Published: 1994-01-25

Substantially Equivalent

Mesa Medical, Inc.

FDA 510(k) clearance K925210 for 90DX MULTITEST METER, MODIFICATION, Substantially Equivalent on 1994-01-25. Applicant: Mesa Medical, Inc.. Device class: 2.

Clearance details

Applicant: Mesa Medical, Inc.
Product code: Code FLB
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1992-10-07
Decision date: 1994-01-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wheat Ridge, CO, US

Download summary PDF View on FDA.gov ↗

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