The following data is part of a premarket notification filed by Intermedics, Inc. with the FDA for Model 483-06 Polyflex Implantable Pacing Lead.
Device ID | K851457 |
510k Number | K851457 |
Device Name: | MODEL 483-06 POLYFLEX IMPLANTABLE PACING LEAD |
Classification | Pacemaker Lead Adaptor |
Applicant | INTERMEDICS, INC. P.O. BOX 617 Freeport, TX 77541 -0617 |
Contact | Lisa S Jones |
Correspondent | Lisa S Jones 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 | 1985-04-11 |
Decision Date | 1985-07-11 |