K-number	K823773
Device name	PROVIAL II #006-010-0201
Applicant	Dynatech Corp.
Product code	KDT
Device class	Class I
Decision date	Jan 21, 1983
Decision	Substantially Equivalent
Regulation	864.3250

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View the full FDA submission: accessdata.fda.gov

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PROVIAL II #006-010-0201

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