2 devices · 2 companies · 2017 to 2025
Product code DSH: Recorder, Magnetic Tape, Medical
2 devices under product code DSH, 2017 to 2025, from 2 companies. Each record carries FDA's decision, the Indications for Use statement verbatim where the public document carries one (2 of 2 here), the regulation, and MAUDE report counts by product code.
Recorder, Magnetic Tape, Medical. 21 CFR 870.2800, Class II. MAUDE held 972 adverse-event reports against this product code as of 2026-10-29; reports are unverified and the code is shared by every device of this type.
Retrieved from FDA public records.
Every device, newest decision first
| Decision | Device | Company | Panel | FDA |
|---|---|---|---|---|
| AT-PatchK242583 · 510(k) | ATsens Co.,Ltd. | Cardiovascular | database entry | |
| Peerbridge CorK171936 · 510(k) | Peerbridge Health INc. | Cardiovascular | database entry |
Every product code in the record, the whole record of FDA AI-enabled medical devices, or what Apodicta does on a medical record.