R2 Corp.
R2 Corp. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 16, 1983.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K832516 | MAGNATRODE CARDIAC MONITORING ELECTRODE | December 16, 1983 |
| K800936 | R2 PADDLE TYPE CABLE-ADAPTOR #S 170,171 | May 23, 1980 |
| K800931 | R2(TM) ECG CABLE-ADAPTOR #'S 120-121-122 | May 23, 1980 |
| K800930 | R2(TM) ECG ELECTRODE SET-#'S305-306 ETC. | May 23, 1980 |
| K800937 | R2 PLATE TYPE CABLE-ADAPTOR #S 175,176 | May 23, 1980 |
| K800932 | ECG-RF-CHOKE CABLE-ADAPTER #'S 121,120 | May 23, 1980 |
| K800935 | R2 APEX-POST.,ANT.&POST. ELECT.(12 MODS) | May 23, 1980 |
| K800934 | R2 ESU CABLE-ADAPTER MODELS 160,161 | May 20, 1980 |
| K800933 | R2 ELECTROSURG. RETURN ELECT. #225ETC. | May 20, 1980 |