The following data is part of a premarket notification filed by Pace Medical with the FDA for Pacemaker Extension Cable Models 4265,4265a, 4265v, 5265, 5265a, 5265v.
Device ID | K002204 |
510k Number | K002204 |
Device Name: | PACEMAKER EXTENSION CABLE MODELS 4265,4265A, 4265V, 5265, 5265A, 5265V |
Classification | Pulse-generator, Pacemaker, External |
Applicant | PACE MEDICAL 391 TOTTEN POND RD. Waltham, MA 02451 |
Contact | Robert C Mace |
Correspondent | Robert C Mace PACE MEDICAL 391 TOTTEN POND RD. Waltham, MA 02451 |
Product Code | DTE |
CFR Regulation Number | 870.3600 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-07-20 |
Decision Date | 2000-10-18 |