AUTOWAND(TM) 7XXX SERIES (K902059) — FDA 510(k) Clearance | Predicase

K-number	K902059
Device name	AUTOWAND(TM) 7XXX SERIES
Applicant	Boehringer Laboratories
Product code	CAC
Device class	Class II
Decision date	Jul 24, 1990
Decision	Substantially Equivalent
Regulation	868.5830

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Source

View the full FDA submission: accessdata.fda.gov

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