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

Substantially Equivalent

Medicorp, Inc.

FDA 510(k) clearance K860026 for ULTRAMAX III, DIALYZER REPROCESSING DEVICE, Substantially Equivalent on 1986-03-14. Applicant: Medicorp, Inc..

Clearance details

Applicant: Medicorp, Inc.
Product code: Code LIF
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

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