The following data is part of a premarket notification filed by Medtronic Vascular with the FDA for Model 5866-37m Lead Adaptor Kit.
| Device ID | K904575 |
| 510k Number | K904575 |
| Device Name: | MODEL 5866-37M LEAD ADAPTOR KIT |
| Classification | Pacemaker Lead Adaptor |
| Applicant | MEDTRONIC VASCULAR 7000 CENTRAL AVE. N.E. Minneapolis, MN 55432 |
| Contact | Norsted, Phd |
| Correspondent | Norsted, Phd MEDTRONIC VASCULAR 7000 CENTRAL AVE. N.E. Minneapolis, MN 55432 |
| Product Code | DTD |
| CFR Regulation Number | 870.3620 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-10-09 |
| Decision Date | 1991-02-01 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00613994897923 | K904575 | 000 |