The following data is part of a premarket notification filed by Pace Medical with the FDA for Pacing Leads Model 3262vu/vb, 3362vu/vb, 3380/3390.
Device ID | K874743 |
510k Number | K874743 |
Device Name: | PACING LEADS MODEL 3262VU/VB, 3362VU/VB, 3380/3390 |
Classification | Permanent Pacemaker Electrode |
Applicant | PACE MEDICAL 391 TOTTEN POND RD. Waltham, MA 02451 |
Contact | Ralph E Hanson |
Correspondent | Ralph E Hanson PACE MEDICAL 391 TOTTEN POND RD. Waltham, MA 02451 |
Product Code | DTB |
CFR Regulation Number | 870.3680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-11-18 |
Decision Date | 1988-01-19 |