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Keller Medical Specialties Products, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K990648KELLER VITAL SIGNS MONITOR, KMS 890+August 10, 1999
K982331KELLER PULSE OXIMETER, MODEL 850+September 11, 1998
K914576KELLER CARDIAC MONITOR MEDIL KMS870December 30, 1991
K910262KELLER VITAL SIGNS MONITOR - KMS-890April 1, 1991
K903437DISPOS ACCESS EXTERNAL CARDIAC PACEMAKERNovember 16, 1990
K895987KELLER PULSE OXIMETER - KMS 850February 22, 1990