ECHO MM1000— 510(k) K834447

Substantially Equivalent

Mesa Medical, Inc.

FDA 510(k) clearance K834447 for ECHO MM1000, Substantially Equivalent on 1984-03-23. Applicant: Mesa Medical, Inc.. Device class: 2.

Clearance details

Applicant: Mesa Medical, Inc.
Product code: Code LIF
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1983-12-16
Decision date: 1984-03-23
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.