The following data is part of a premarket notification filed by Cardiac Assist Devices, Inc. with the FDA for Magno Alarm.
| Device ID | K960849 |
| 510k Number | K960849 |
| Device Name: | MAGNO ALARM |
| Classification | Magnet, Test, Pacemaker |
| Applicant | CARDIAC ASSIST DEVICES, INC. 11000 CEDAR AVE., SUITE 451 Cleveland, OH 44106 -3052 |
| Contact | Rassoll Rashidi |
| Correspondent | Rassoll Rashidi CARDIAC ASSIST DEVICES, INC. 11000 CEDAR AVE., SUITE 451 Cleveland, OH 44106 -3052 |
| Product Code | DTG |
| CFR Regulation Number | 870.3690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-02-20 |
| Decision Date | 1997-03-26 |
| Summary: | summary |