The following data is part of a premarket notification filed by Lectec Corp. with the FDA for Lectec Stimulating Electrode.
| Device ID | K872250 |
| 510k Number | K872250 |
| Device Name: | LECTEC STIMULATING ELECTRODE |
| Classification | Electrode, Cutaneous |
| Applicant | LECTEC CORP. 10701 RED CIRCLE DR. Minnetonka, MN 55343 |
| Contact | David Montecalvo |
| Correspondent | David Montecalvo LECTEC CORP. 10701 RED CIRCLE DR. Minnetonka, MN 55343 |
| Product Code | GXY |
| CFR Regulation Number | 882.1320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-06-12 |
| Decision Date | 1987-08-07 |