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K & S Medicorp
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K862131
SALTZMAN EAR(TM) ENDOTRACHEAL ASCULTATION RECEPTOR
July 14, 1986
K854772
TRANSCOR (TM) RADIO-STETHOSCOPE
May 13, 1986
K854771
SALTZMAN STETHOSCOPE HEAD
May 9, 1986