Surgidyne, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K892334LEONARD TUBEMay 31, 1989
K883582VARIDYNE MODEL 250 SUCTION DRAINAGE SYSTEMOctober 3, 1988
K864822VARIDYNE 550, MODELS 12E,12M,24E & 24M SUCTION SYSJanuary 15, 1987
K860030SURGIDYNE VARIDYNE, MODEL 140-2I & MODEL 140-2IDFebruary 12, 1986
K852180SURGIDYNES VARIDYNE 350-2I & 350-2C CORDLESS ELEC.July 1, 1985
K850634SURGIDYNE SURGIFLO C.W.S. DRAIN PRODUCTSJune 28, 1985