R2 Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K832516MAGNATRODE CARDIAC MONITORING ELECTRODEDecember 16, 1983
K800931R2(TM) ECG CABLE-ADAPTOR #'S 120-121-122May 23, 1980
K800935R2 APEX-POST.,ANT.&POST. ELECT.(12 MODS)May 23, 1980
K800937R2 PLATE TYPE CABLE-ADAPTOR #S 175,176May 23, 1980
K800932ECG-RF-CHOKE CABLE-ADAPTER #'S 121,120May 23, 1980
K800930R2(TM) ECG ELECTRODE SET-#'S305-306 ETC.May 23, 1980
K800936R2 PADDLE TYPE CABLE-ADAPTOR #S 170,171May 23, 1980
K800933R2 ELECTROSURG. RETURN ELECT. #225ETC.May 20, 1980
K800934R2 ESU CABLE-ADAPTER MODELS 160,161May 20, 1980