FDA 510(k) Application Details - K936006

Device Classification Name	Viscometer, Mucus, Cervical   More FDA Info for this Device
510(K) Number	K936006
Device Name	Viscometer, Mucus, Cervical
Applicant	HAROLD J. KOSASKY, M.D. 25 BOYLSTON ST. CHESTNUT HILL, MA 02167 US Other 510(k) Applications for this Company
Contact	HAROLD J KOSASKY Other 510(k) Applications for this Contact
Regulation Number	884.1040   More FDA Info for this Regulation Number
Classification Product Code	LHZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/15/1993
Decision Date	02/09/1996
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