Medical Device Manufacturer · US , Mchenry , IL

R2 Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1980

Total

Cleared

Denied

R2 Corp. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1980 to 1983. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by R2 Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by R2 Corp.

9 devices

1-9 of 9

Cleared Dec 16, 1983

MAGNATRODE CARDIAC MONITORING ELECTRODE

K832516 · DRX

Cardiovascular · 141d

Cleared May 23, 1980

R2(TM) ECG ELECTRODE SET-#'S305-306 ETC.

K800930 · DRX

Cardiovascular · 32d

Cleared May 23, 1980

R2(TM) ECG CABLE-ADAPTOR #'S 120-121-122

K800931 · DSA

Cardiovascular · 32d

Cleared May 23, 1980

ECG-RF-CHOKE CABLE-ADAPTER #'S 121,120

K800932 · DSA

Cardiovascular · 32d

Cleared May 23, 1980

R2 APEX-POST.,ANT.&POST. ELECT.(12 MODS)

K800935 · DRX

Cardiovascular · 32d

Cleared May 23, 1980

R2 PADDLE TYPE CABLE-ADAPTOR #S 170,171

K800936 · LDD

Cardiovascular · 32d

Cleared May 23, 1980

R2 PLATE TYPE CABLE-ADAPTOR #S 175,176

K800937 · LDD

Cardiovascular · 32d

Cleared May 20, 1980

R2 ELECTROSURG. RETURN ELECT. #225ETC.

K800933 · JOT

General & Plastic Surgery · 29d

Cleared May 20, 1980

R2 ESU CABLE-ADAPTER MODELS 160,161

K800934 · IKD

Physical Medicine · 29d

R2 Corp. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by R2 Corp.

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