K-number	K851780
Device name	25-230 TO 25-390 VARIOUS NEEDLE HOLDERS
Applicant	Artiberia
Product code	FHQ
Device class	Class I
Decision date	Jun 20, 1985
Decision	Substantially Equivalent
Regulation	876.4730

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View the full FDA submission: accessdata.fda.gov

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25-230 TO 25-390 VARIOUS NEEDLE HOLDERS

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