The following data is part of a premarket notification filed by Telectronics, Inc. with the FDA for Qmplantable Program. Cardiac Pulse Gen. W/telemetr.
| Device ID | K850252 |
| 510k Number | K850252 |
| Device Name: | QMPLANTABLE PROGRAM. CARDIAC PULSE GEN. W/TELEMETR |
| Classification | Implantable Pacemaker Pulse-generator |
| 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 | DXY |
| CFR Regulation Number | 870.3610 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-01-22 |
| Decision Date | 1985-04-04 |