The following data is part of a premarket notification filed by Matrix Electromedical, Inc. with the FDA for Matrix Pro-elecdt.
| Device ID | K930263 |
| 510k Number | K930263 |
| Device Name: | MATRIX PRO-ELECDT |
| Classification | Interferential Current Therapy |
| Applicant | MATRIX ELECTROMEDICAL, INC. 9545 BONITA VISTA ST. Las Vegas, NV 89131 |
| Contact | Deborah Sorgnard |
| Correspondent | Deborah Sorgnard MATRIX ELECTROMEDICAL, INC. 9545 BONITA VISTA ST. Las Vegas, NV 89131 |
| Product Code | LIH |
| CFR Regulation Number | 882.5890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-01-19 |
| Decision Date | 1994-06-09 |