The following data is part of a premarket notification filed by Progressive Electrical Therapeutics with the FDA for The Signature Series, M Iv.
| Device ID | K933197 |
| 510k Number | K933197 |
| Device Name: | THE SIGNATURE SERIES, M IV |
| Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
| Applicant | PROGRESSIVE ELECTRICAL THERAPEUTICS 122 W. WALNUT Nevada, MO 64772 |
| Contact | Gary Huddleston |
| Correspondent | Gary Huddleston PROGRESSIVE ELECTRICAL THERAPEUTICS 122 W. WALNUT Nevada, MO 64772 |
| Product Code | GZJ |
| CFR Regulation Number | 882.5890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-07-01 |
| Decision Date | 1995-06-02 |