FDA 510(k) Application Details - K952569

Device Classification Name	Apparatus, Cautery, Radiofrequency, Ac-Powered   More FDA Info for this Device
510(K) Number	K952569
Device Name	Apparatus, Cautery, Radiofrequency, Ac-Powered
Applicant	GAMP & ASSOC. 3237 HAAS BRIDGETON, MO 63044 US Other 510(k) Applications for this Company
Contact	JAMES TAYLOR Other 510(k) Applications for this Contact
Regulation Number	886.4100   More FDA Info for this Regulation Number
Classification Product Code	HQR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/05/1995
Decision Date	01/05/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review