K-number	K993545
Device name	TENAX WHITE POST
Applicant	Coltene/Whaledent, Inc.
Product code	ELR
Device class	Class I
Decision date	Apr 14, 2000
Decision	Substantially Equivalent
Regulation	872.3810

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Source

View the full FDA submission: accessdata.fda.gov

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TENAX WHITE POST

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