The following data is part of a premarket notification filed by Labeltape Meditect, Inc. with the FDA for Foam Bordered Diagnostic (care) Electrode.
| Device ID | K875041 |
| 510k Number | K875041 |
| Device Name: | FOAM BORDERED DIAGNOSTIC (CARE) ELECTRODE |
| Classification | Electrode, Electrocardiograph |
| Applicant | LABELTAPE MEDITECT, INC. 4275 AIRWEST DR., S.E. P.O. BOX 8823 Grand Rapids, MI 49508 |
| Contact | Michael S Bartlett |
| Correspondent | Michael S Bartlett LABELTAPE MEDITECT, INC. 4275 AIRWEST DR., S.E. P.O. BOX 8823 Grand Rapids, MI 49508 |
| Product Code | DRX |
| CFR Regulation Number | 870.2360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-12-03 |
| Decision Date | 1988-01-28 |