Syntex Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K920314TXIT D.A.U. BARBITURATE ASSAY (MODIFICATION)April 17, 1992
K843593SURGIPRESS SURGICAL LOOPOctober 24, 1984
K780997AMALGAM ALLOYJuly 27, 1978
K780769S-100 CT SCANNERJune 2, 1978
K780483FIBER OPTIC HANDPIECEApril 28, 1978
K761331OPUS I OPTION - FIBER OPTIC L SYSTEMJanuary 3, 1977
K761330SYNTEX SYSTEM 6000December 30, 1976
K761332HI-SENSITIVITY MODE OPTION FOR S60-1ADecember 30, 1976
K761264OPTIONS FOR STAR DENTAL OPUS IDecember 23, 1976
K761033COMPUTERIZED TOMOGRAPHY SCANNERNovember 24, 1976