K832272 is an FDA 510(k) clearance for the TOURNIQUET CUFF PRESSURE MONITOR #TCPM..
Submitted by Electromedics, Inc.. The FDA issued a Cleared decision on November 28, 1983, 139 days after receiving the submission on July 12, 1983.
This device falls under the General & Plastic Surgery FDA review panel.
| 510(k) Number | K832272 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 12, 1983 |
| Decision Date | November 28, 1983 |
| Days to Decision | 139 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | LDQ |
| Device Class | — |