Lares Manufacturing Co., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K831351PERMALUX VISIBLE CURE COMPOSITE RESTORNovember 14, 1983
K801535LARES HANDPIECE OILDecember 16, 1980
K801592FIBER OPTIC HOSEJuly 21, 1980
K801591FIBER OPTIC ILLUMINATORJuly 21, 1980
K801534LARES AIR PRESSURE GAUGEJuly 14, 1980
K780038DENTAL HANDPIECEJanuary 20, 1978