FDA 510(k) Application Details - K961959

Device Classification Name	Needle, Aspiration And Injection, Disposable   More FDA Info for this Device
510(K) Number	K961959
Device Name	Needle, Aspiration And Injection, Disposable
Applicant	MEDICAL DEVICE TECHNOLOGIES, INC. 4445 SW 35TH TERRACE SUITE 310 GAINESVILLE, FL 32608 US Other 510(k) Applications for this Company
Contact	KARL SWARTZ Other 510(k) Applications for this Contact
Regulation Number	878.4800   More FDA Info for this Regulation Number
Classification Product Code	GAA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/20/1996
Decision Date	07/19/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review