AUTOWAND(TM) 7XXX SERIES, MODIFICATION (K904888) — FDA 510(k) Clearance | Predicase

K-number	K904888
Device name	AUTOWAND(TM) 7XXX SERIES, MODIFICATION
Applicant	Boehringer Laboratories
Product code	CAC
Device class	Class II
Decision date	Jan 16, 1991
Decision	Substantially Equivalent
Regulation	868.5830

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Source

View the full FDA submission: accessdata.fda.gov

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