The following data is part of a premarket notification filed by Telectronics Pacing Systems, Inc. with the FDA for Optima Series Ii Model 147b Single Chamber Pulse.
Device ID | K903186 |
510k Number | K903186 |
Device Name: | OPTIMA SERIES II MODEL 147B SINGLE CHAMBER PULSE |
Classification | Implantable Pacemaker Pulse-generator |
Applicant | TELECTRONICS PACING SYSTEMS, INC. 7400 SOUTH TUCSON WAY Englewood, CO 80112 |
Contact | Duane A Schultz |
Correspondent | Duane A Schultz TELECTRONICS PACING SYSTEMS, INC. 7400 SOUTH TUCSON WAY Englewood, CO 80112 |
Product Code | DXY |
CFR Regulation Number | 870.3610 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-07-19 |
Decision Date | 1991-01-18 |