K & S Medicorp

FDA Regulatory Profile

K & S Medicorp appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 14, 1986.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K862131SALTZMAN EAR(TM) ENDOTRACHEAL ASCULTATION RECEPTORJuly 14, 1986
K854772TRANSCOR (TM) RADIO-STETHOSCOPEMay 13, 1986
K854771SALTZMAN STETHOSCOPE HEADMay 9, 1986