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Rabar, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K844017
MICROTENS 7757 T.E.N.S. STIMULATOR
November 30, 1984
K842414
ECHO PULSE BURST
July 27, 1984
K821736
ECHO-PULSE KM555
December 9, 1982