The following data is part of a premarket notification filed by Magstim Corporation Us with the FDA for Magstim Rapid.
| Device ID | K992911 |
| 510k Number | K992911 |
| Device Name: | MAGSTIM RAPID |
| Classification | Stimulator, Electrical, Evoked Response |
| Applicant | MAGSTIM CORPORATION US 730 FIFTH AVE. 9TH FLOOR New York, NY 10019 |
| Contact | Reza Jalinous |
| Correspondent | Reza Jalinous MAGSTIM CORPORATION US 730 FIFTH AVE. 9TH FLOOR New York, NY 10019 |
| Product Code | GWF |
| CFR Regulation Number | 882.1870 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-08-30 |
| Decision Date | 2000-01-07 |