K-number	K991526
Device name	ISOSTAR I-125 INTERSTITIAL SEED, MODEL IS-12501
Applicant	Imagyn Medical Technologies, Inc.
Product code	KXK
Device class	Class II
Decision date	Jun 17, 1999
Decision	Substantially Equivalent
Regulation	892.5730

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View the full FDA submission: accessdata.fda.gov

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ISOSTAR I-125 INTERSTITIAL SEED, MODEL IS-12501

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