FDA 510(k) Application Details - K014246

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K014246
Device Name	Anesthesia Conduction Kit
Applicant	AVID N.I.T., INC. 390 SCARLET BLVD. OLDSMAR, FL 34677 US Other 510(k) Applications for this Company
Contact	SCOTT HENDERSON Other 510(k) Applications for this Contact
Regulation Number	868.5140   More FDA Info for this Regulation Number
Classification Product Code	CAZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/26/2001
Decision Date	07/16/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review