NEGATOVE PRESSURE CONVERTOR— 510(k) K791164

Substantially Equivalent

Medicorp, Inc.

FDA 510(k) clearance K791164 for NEGATOVE PRESSURE CONVERTOR, Substantially Equivalent on 1979-10-04. Applicant: Medicorp, Inc.. Device class: 2.

Clearance details

Applicant: Medicorp, Inc.
Product code: Code FLC
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1979-06-25
Decision date: 1979-10-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Medicorp, Inc.

K860026 — ULTRAMAX III, DIALYZER REPROCESSING DEVICE1986-03-14
K844850 — MEDICORP DEHYDRACON A DEHYDRATED DIALYSATE CONCENT1985-04-02
K832705 — ULTRAMAX1984-06-25
K791396 — MEDI-TRAK PORTABLE TRACTION DEVICE1979-08-16

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