K-number	K911202
Device name	ATRAUMATIC STANDARD SPROTTE NEEDLE
Applicant	Pajunk GmbH
Product code	BSP
Device class	Class II
Decision date	May 4, 1992
Decision	Substantially Equivalent
Regulation	868.5150

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Source

View the full FDA submission: accessdata.fda.gov

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ATRAUMATIC STANDARD SPROTTE NEEDLE

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