FDA 510(k) Application Details - K963747

Device Classification Name	Pick, Massaging   More FDA Info for this Device
510(K) Number	K963747
Device Name	Pick, Massaging
Applicant	WHITEHILL MANUFACTURING, INC. 950 HWY. 36 HAZLET, NJ 07730 US Other 510(k) Applications for this Company
Contact	PETER P WALTERS Other 510(k) Applications for this Contact
Regulation Number	872.6650   More FDA Info for this Regulation Number
Classification Product Code	JET Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/17/1996
Decision Date	12/16/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review