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Rmp Co.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K981844
SLEEP MANAGEMENT SYSTEM
August 7, 1998
K862197
RMP COMPANT CRICOTHYROTOMY EQUIPMENT STORAGE TRAY
June 19, 1986
K862154
VENESECTION EQUIPMENT STORAGE TRAY
June 16, 1986
K832697
RMP INTUBATION EQUIP. STORAGE TRAY
December 27, 1983