MODEL 90DX MULTITEST METER— 510(k) K882032

Substantially Equivalent

Mesa Medical, Inc.

FDA 510(k) clearance K882032 for MODEL 90DX MULTITEST METER, Substantially Equivalent on 1988-08-11. 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: 1988-05-16
Decision date: 1988-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wheat Ridge, CO, 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.