FDA 510(k) Application Details - K981260

Device Classification Name	Extractor, Vacuum, Fetal   More FDA Info for this Device
510(K) Number	K981260
Device Name	Extractor, Vacuum, Fetal
Applicant	CLINICAL INNOVATIONS, INC. 6477 SOUTH COTTONWOOD ST. MURRAY, UT 84107 US Other 510(k) Applications for this Company
Contact	WM D WALLACE Other 510(k) Applications for this Contact
Regulation Number	884.4340   More FDA Info for this Regulation Number
Classification Product Code	HDB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/06/1998
Decision Date	09/22/1998
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