ULTRAMAX III, DIALYZER REPROCESSING DEVICE— 510(k) K860026

Name: FDA 510(k) clearance K860026
Creator: U.S. Food and Drug Administration
Published: 1986-03-14

Substantially Equivalent

Medicorp, Inc.

FDA 510(k) clearance K860026 for ULTRAMAX III, DIALYZER REPROCESSING DEVICE, Substantially Equivalent on 1986-03-14. 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: 1986-01-03
Decision date: 1986-03-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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