K-number	K884181
Device name	MANUAL SURGICAL INSTRUMENTS (SEVERAL MODELS)
Applicant	Sales & Marketing Assoc.
Product code	GEN
Device class	Class I
Decision date	Nov 10, 1988
Decision	Substantially Equivalent
Regulation	878.4800

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Source

View the full FDA submission: accessdata.fda.gov

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MANUAL SURGICAL INSTRUMENTS (SEVERAL MODELS)

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