The following data is part of a premarket notification filed by Medtronic Vascular with the FDA for Medical Safety Cable And Lead System.
| Device ID | K912415 |
| 510k Number | K912415 |
| Device Name: | MEDICAL SAFETY CABLE AND LEAD SYSTEM |
| Classification | Monitor, Breathing Frequency |
| Applicant | MEDTRONIC VASCULAR 60 NEWARK ST. Haverhill, MA 01830 |
| Contact | Janice M Pevide |
| Correspondent | Janice M Pevide MEDTRONIC VASCULAR 60 NEWARK ST. Haverhill, MA 01830 |
| Product Code | BZQ |
| CFR Regulation Number | 868.2375 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-05-31 |
| Decision Date | 1991-08-16 |