K-number	K914221
Device name	KPE 220 TS, NONSTERILE
Applicant	Ipax, Inc.
Product code	HQE
Device class	Class II
Decision date	Oct 25, 1991
Decision	Substantially Equivalent
Regulation	886.4150

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View the full FDA submission: accessdata.fda.gov

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KPE 220 TS, NONSTERILE

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