FDA 510(k) Application Details - K970078

Device Classification Name	Insufflator, Hysteroscopic   More FDA Info for this Device
510(K) Number	K970078
Device Name	Insufflator, Hysteroscopic
Applicant	DAVOL, INC., SUB. C.R. BARD, INC. 100 SOCKANOSSETT CROSSROAD CRANSTON, RI 02920 US Other 510(k) Applications for this Company
Contact	ROBIN M DRAGO Other 510(k) Applications for this Contact
Regulation Number	884.1700   More FDA Info for this Regulation Number
Classification Product Code	HIG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/09/1997
Decision Date	12/11/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review