K-number	K882013
Device name	SOFT TISSUE BIOPSY DEVICE
Applicant	Ocean Medical Products, Ltd.
Product code	DWO
Device class	Class I
Decision date	Jun 15, 1988
Decision	Substantially Equivalent
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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SOFT TISSUE BIOPSY DEVICE

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