The following data is part of a premarket notification filed by Marquette Electronics, Inc. with the FDA for Cardioserv S.
| Device ID | K962551 |
| 510k Number | K962551 |
| Device Name: | CARDIOSERV S |
| Classification | Dc-defibrillator, Low-energy, (including Paddles) |
| Applicant | MARQUETTE ELECTRONICS, INC. 8200 WEST TOWER AVE. Milwaukee, WI 53223 |
| Contact | Kristin Pabst |
| Correspondent | Kristin Pabst MARQUETTE ELECTRONICS, INC. 8200 WEST TOWER AVE. Milwaukee, WI 53223 |
| Product Code | LDD |
| CFR Regulation Number | 870.5300 [🔎] |
| Decision | Se Subject To Tracking Reg (ST) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-06-28 |
| Decision Date | 1996-11-19 |
| Summary: | summary |