K-number	K790854
Device name	FORCEPS #101 AND #102
Applicant	C. Intl.
Product code	GEN
Device class	Class I
Decision date	Jun 5, 1979
Decision	Substantially Equivalent
Regulation	878.4800

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Source

View the full FDA submission: accessdata.fda.gov

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FORCEPS #101 AND #102

Everything you need for a 510(k) submission. Nothing you don't.