K-number	K920263
Device name	MANUAL SURGICAL INSTRUMENTS
Applicant	Phoenix Instruments Div.
Product code	KDC
Device class	Class I
Decision date	May 6, 1992
Decision	Substantially Equivalent
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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MANUAL SURGICAL INSTRUMENTS

Everything you need for a 510(k) submission. Nothing you don't.