K-number	K924958
Device name	BIOPSY/MYELO/ARTHRO/AMNIOCENT/BASIC SKIN PREP TRAY
Applicant	Medical Insights, Inc.
Product code	KDD
Device class	Class I
Decision date	Jun 7, 1993
Decision	Substantially Equivalent — Kit Device
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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BIOPSY/MYELO/ARTHRO/AMNIOCENT/BASIC SKIN PREP TRAY

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