ULTRAMAX— 510(k) K832705

Substantially Equivalent

Medicorp, Inc.

FDA 510(k) clearance K832705 for ULTRAMAX, Substantially Equivalent on 1984-06-25. Applicant: Medicorp, Inc.. Device class: 2.

Clearance details

Applicant: Medicorp, Inc.
Product code: Code LIF
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1983-08-12
Decision date: 1984-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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More clearances from Medicorp, Inc.

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Data sourced from openFDA. This site is unofficial and independent of the FDA.