FDA 510(k) Application Details - K081420

Device Classification Name	Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days   More FDA Info for this Device
510(K) Number	K081420
Device Name	Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days
Applicant	RETRACTABLE TECHNOLOGIES, INC. 511 LOBO LN. LITTLE ELM, TX 75068-0009 US Other 510(k) Applications for this Company
Contact	RHONDA WELLS Other 510(k) Applications for this Contact
Regulation Number	880.5200   More FDA Info for this Regulation Number
Classification Product Code	FOZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/20/2008
Decision Date	11/07/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review