SECURATRODE
Electrode, Electrocardiograph
MEDDEV INTERNATIONAL CORP.
The following data is part of a premarket notification filed by Meddev International Corp. with the FDA for Securatrode.
Pre-market Notification Details
| Device ID | K874562 |
| 510k Number | K874562 |
| Device Name: | SECURATRODE |
| Classification | Electrode, Electrocardiograph |
| Applicant | MEDDEV INTERNATIONAL CORP. P.O. BOX 1352 Los Altos, CA 94023 -1352 |
| Contact | Jeffrey L Wisnicki |
| Correspondent | Jeffrey L Wisnicki MEDDEV INTERNATIONAL CORP. P.O. BOX 1352 Los Altos, CA 94023 -1352 |
| Product Code | DRX |
| CFR Regulation Number | 870.2360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-11-04 |
| Decision Date | 1988-01-28 |
Trademark Results [SECURATRODE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SECURATRODE 74086736 1652984 Dead/Cancelled |
MEDDEV CORPORATION 1990-08-10 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.