The following data is part of a premarket notification filed by Acutus Medical, Inc. with the FDA for Acqmap High Resolution Imaging And Mapping System.
| Device ID | K220784 |
| 510k Number | K220784 |
| Device Name: | AcQMap High Resolution Imaging And Mapping System |
| Classification | Computer, Diagnostic, Programmable |
| Applicant | Acutus Medical, Inc. 2210 Faraday Ave, Suite 100 Carlsbad, CA 92008 |
| Contact | Sindhu Sridhar |
| Correspondent | Karla Schaffner Acutus Medical, Inc. 2210 Faraday Ave, Suite 100 Carlsbad, CA 92008 |
| Product Code | DQK |
| Subsequent Product Code | ITX |
| Subsequent Product Code | IYO |
| CFR Regulation Number | 870.1425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2022-03-17 |
| Decision Date | 2022-07-01 |