The following data is part of a premarket notification filed by Lectec Corp. with the FDA for Md Monitoring/diagnostic Electrode.
| Device ID | K870873 |
| 510k Number | K870873 |
| Device Name: | MD MONITORING/DIAGNOSTIC ELECTRODE |
| Classification | Electrode, Electrocardiograph |
| 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 | DRX |
| CFR Regulation Number | 870.2360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-03-03 |
| Decision Date | 1987-04-10 |