The following data is part of a premarket notification filed by Medtronic Vascular with the FDA for Model 2872 Bipolar Lead Adaptor Kit.
| Device ID | K982220 |
| 510k Number | K982220 |
| Device Name: | MODEL 2872 BIPOLAR LEAD ADAPTOR KIT |
| Classification | Pacemaker Lead Adaptor |
| Applicant | MEDTRONIC VASCULAR 7000 CENTRAL AVE. NE Minneapolis, MN 55432 -3576 |
| Contact | Brian J Edwards |
| Correspondent | Brian J Edwards MEDTRONIC VASCULAR 7000 CENTRAL AVE. NE Minneapolis, MN 55432 -3576 |
| Product Code | DTD |
| CFR Regulation Number | 870.3620 [🔎] |
| Decision | Se Subject To Tracking Reg (ST) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-06-24 |
| Decision Date | 1998-10-15 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00681490064583 | K982220 | 000 |