The following data is part of a premarket notification filed by Intermedics, Inc. with the FDA for Biopore 493-05 Endocardial Implantable Pacing Lead.
| Device ID | K844814 |
| 510k Number | K844814 |
| Device Name: | BIOPORE 493-05 ENDOCARDIAL IMPLANTABLE PACING LEAD |
| Classification | Pacemaker Lead Adaptor |
| Applicant | INTERMEDICS, INC. P.O. BOX 617 Freeport, TX 77541 -0617 |
| Contact | David M Makanani |
| Correspondent | David M Makanani INTERMEDICS, INC. P.O. BOX 617 Freeport, TX 77541 -0617 |
| Product Code | DTD |
| CFR Regulation Number | 870.3620 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-12-11 |
| Decision Date | 1985-08-29 |