The following data is part of a premarket notification filed by Marquette Electronics, Inc. with the FDA for Series 1500 Responder.
| Device ID | K902782 |
| 510k Number | K902782 |
| Device Name: | SERIES 1500 RESPONDER |
| Classification | Dc-defibrillator, Low-energy, (including Paddles) |
| Applicant | MARQUETTE ELECTRONICS, INC. 8200 WEST TOWER AVE. Milwaukee, WI 53223 |
| Contact | Sandra L Schick |
| Correspondent | Sandra L Schick MARQUETTE ELECTRONICS, INC. 8200 WEST TOWER AVE. Milwaukee, WI 53223 |
| Product Code | LDD |
| CFR Regulation Number | 870.5300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-06-26 |
| Decision Date | 1991-01-18 |