K-number	K914241
Device name	PIONEER PRO-PUMP DUAL CONTROL
Applicant	Pioneer Medical, Inc.
Product code	HHK
Device class	Class II
Decision date	Mar 4, 1992
Decision	Substantially Equivalent
Regulation	884.1175

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View the full FDA submission: accessdata.fda.gov

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PIONEER PRO-PUMP DUAL CONTROL

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