K-number	K760174
Device name	ADAPTER, RESECTOSCOPE
Applicant	V. Mueller O.V. Baxter Healthcare Corp.
Product code	FDC
Device class	Class II
Decision date	Aug 30, 1976
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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ADAPTER, RESECTOSCOPE

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