K-number	K890380
Device name	CERVICAL BIOPSY FORCEPS
Applicant	Kinetic Medical Products
Product code	HFB
Device class	Class I
Decision date	Feb 27, 1989
Decision	Substantially Equivalent
Regulation	884.4530

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View the full FDA submission: accessdata.fda.gov

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CERVICAL BIOPSY FORCEPS

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