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 |