K-number	K951753
Device name	MEDTEC AUTOBLOT 2000
Applicant	Medtec, Inc.
Product code	JQW
Device class	Class I
Decision date	Oct 17, 1995
Decision	Substantially Equivalent
Regulation	862.2750

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View the full FDA submission: accessdata.fda.gov

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MEDTEC AUTOBLOT 2000

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