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Teknomed, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K925395TECHNOMED PULSOLITH 4000 LASER SYSTEMMay 21, 1993
K920708MULTILASE 2500 ANovember 5, 1992
K913917MULTILASE 2100 C, 2100 DNovember 5, 1992
K913290MULTILASE 2100 AFebruary 21, 1992
K895178TECHNOMED PULSOLITH LASER SYSTEMOctober 6, 1989
K890436TECHNOMED PULSOLITH LASER SYSTEMMarch 23, 1989
K790132TECNOTOMOFebruary 21, 1979