K-number	K920104
Device name	IDENTI LOOPS DEGANIA SILICONE
Applicant	Puritas Health Care, Inc.
Product code	DSS
Device class	Class II
Decision date	Apr 20, 1992
Decision	Substantially Equivalent
Regulation	870.3250

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View the full FDA submission: accessdata.fda.gov

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IDENTI LOOPS DEGANIA SILICONE

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