K-number	K874145
Device name	TITAN GEL REP LDH-6 HV
Applicant	Helena Laboratories
Product code	CFE
Device class	Class II
Decision date	Nov 24, 1987
Decision	Substantially Equivalent
Regulation	862.1445

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View the full FDA submission: accessdata.fda.gov

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TITAN GEL REP LDH-6 HV

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