K-number	K823229
Device name	SUTURE NEEDLES
Applicant	Feuerstein Produktions
Product code	—
Device class	Class unclassified
Decision date	Feb 18, 1983
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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SUTURE NEEDLES

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