MEDO MEDOMER MBF-100 II— 510(k) K841235

Substantially Equivalent

Medo U.S.A., Inc.

FDA 510(k) clearance K841235 for MEDO MEDOMER MBF-100 II, Substantially Equivalent on 1984-11-19. Applicant: Medo U.S.A., Inc.. Device class: 2.

Clearance details

Applicant: Medo U.S.A., Inc.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 1984-03-22
Decision date: 1984-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wood Dale, 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.