PIONEER PRO-PUMP DUAL CONTROL— 510(k) K914241

Name: FDA 510(k) clearance K914241
Creator: U.S. Food and Drug Administration
Published: 1992-03-04

Substantially Equivalent

Pioneer Medical, Inc.

FDA 510(k) clearance K914241 for PIONEER PRO-PUMP DUAL CONTROL, Substantially Equivalent on 1992-03-04. Applicant: Pioneer Medical, Inc.. Device class: 2.

Clearance details

Applicant: Pioneer Medical, Inc.
Product code: Code HHK
Device class: Class 2
Regulation: 21 CFR 884.1175
Advisory panel: Obstetrics/Gynecology
Date received: 1991-09-23
Decision date: 1992-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Branford, CT, US

Download summary PDF View on FDA.gov ↗

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