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

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..

Clearance details

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

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