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 | K193013 |
510k Number | K193013 |
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 | Karla Schaffner |
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 | 2019-10-29 |
Decision Date | 2020-02-11 |