K-number	K896589
Device name	MANUAL SURGICAL INSTRUMENTS FOR TITAMED ANTWERP
Applicant	Optik
Product code	LRZ
Device class	Class I
Decision date	Dec 27, 1989
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 FOR TITAMED ANTWERP

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