FDA 510(k) Application Details - K091937

Device Classification Name	Speculum, Vaginal, Nonmetal   More FDA Info for this Device
510(K) Number	K091937
Device Name	Speculum, Vaginal, Nonmetal
Applicant	OBP CORPORATION 360 MERRIMACK STREET BUILDING 9 LAWRENCE, MA 01843 US Other 510(k) Applications for this Company
Contact	KEITH ISAACSON Other 510(k) Applications for this Contact
Regulation Number	884.4530   More FDA Info for this Regulation Number
Classification Product Code	HIB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/30/2009
Decision Date	09/09/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review