K-number	K102029
Device name	PEAK PULSAR II GENERATOR MODEL PS100-102
Applicant	Peak Surgical, Inc.
Product code	GEI
Device class	Class II
Decision date	Dec 16, 2010
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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PEAK PULSAR II GENERATOR MODEL PS100-102

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