Pacemaker Lead Adapter
by Cordis Corp.
510(k) K862656
Pacemaker Lead Adapter is a Class II device made by Cordis Corp., cleared under FDA 510(k) K862656 on 30 Jul 1986, active as of 9 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK862656 | Date30 Jul 1986 | StatusActive |
Official records
- FDA 510(k) database K862656
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- DTD
- Device class
- Class II
- Regulation
- 21 CFR Part 870.3620
- Advisory committee
- Cardiovascular
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code DTD (Pacemaker Lead Adaptor).
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- Endocardial Firm Lead by Pacesetter Systems
- Model 5866-37M Lead Adaptor Kit by MEDTRONIC VASCULAR, INC.
- Sentra Pacemaker Lead Adaptor by Cardiac Pacemakers, Inc.
- Implantable Electrode Unipolar Adapt by Telectronics, Inc.
- CCS Model AV-106 Implantable A-V Data Lead by Cardiac Control Systems, Inc.
- Electrode Lead Model 030-198 by Telectronics, Inc.