The following data is part of a premarket notification filed by Telectronics, Inc. with the FDA for Implant Elect Lead, Mod 30-403 Using Polyu 90 A.
Device ID | K852709 |
510k Number | K852709 |
Device Name: | IMPLANT ELECT LEAD, MOD 30-403 USING POLYU 90 A |
Classification | Permanent Pacemaker Electrode |
Applicant | TELECTRONICS, INC. 40 CRANE HILL RD. Suffield, CT 06078 |
Contact | William C Nealon |
Correspondent | William C Nealon TELECTRONICS, INC. 40 CRANE HILL RD. Suffield, CT 06078 |
Product Code | DTB |
CFR Regulation Number | 870.3680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-06-26 |
Decision Date | 1985-09-17 |