GC85A
FDA 510(k) K260481 · Samsung Electronics Co., Ltd.
510(k) numberK260481
Submission
- Device name
- GC85A
- Applicant
- Samsung Electronics Co., Ltd.
Suwon-Si, KR - Received
- February 13, 2026
- Decision date
- August 27, 2026
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K260227 | EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS…KPR · Traditional | DRTECH Corporation | 09/08/2026SE |
| K260488 | MULTIX Impact; MULTIX Impact CKPR · Traditional | Siemens Medical Solutions USA, Inc. | 08/31/2026SE |
| K260482 | DRE DuoKPR · Traditional | Jpi Healthcare Co, Ltd. | 06/15/2026SE |
| K253446 | AeroDR TX c02KPR · Traditional | Dk Medical Systems Co., Ltd. | 04/10/2026SE |
| K250954 | DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector…KPR · Traditional | Carestream Health | 01/20/2026SE |
| K252000 | uDR Arria & uDR ArisKPR · Traditional | Shanghai United Imaging Healthcare Co., Ltd. | 11/26/2025SE |
| K251167 | uDR Aurora CXKPR · Traditional | Shanghai United Imaging Healthcare Co., Ltd. | 09/19/2025SE |
| K250788 | Definium Tempo SelectKPR · Traditional | Ge Hualun Medical Systems Co. , Ltd. | 08/28/2025SE |
| K250790 | Innovision-DxiiKPR · Traditional | Dk Medical Systems Co., Ltd. | 08/01/2025SE |
| K250738 | YSIO X.preeKPR · Traditional | Siemens Medical Solutions | 07/31/2025SE |
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| K242478 | GF85 (models GF85-3P, GF85-SP)KPR · Traditional | 09/19/2024SE |
| K240909 | Samsung ECG App v 1.3 (ECG)QDA · Traditional | 08/02/2024SE |
| K230292 | Samsung ECG Monitor Application with Irregular Heart Rhythm NotificationQDA · Traditional | 05/02/2023SE |
| K222353 | GM85IZL · Traditional | 09/29/2022SE |
| K220175 | GM85IZL · Traditional | 04/21/2022SE |
| K213452 | Gems-HPHL · Traditional | 04/21/2022SE |
| K211139 | CUBE Air PurifierFRA · Traditional | 11/26/2021SE |
Questions and answers
When was GC85A cleared by the FDA?
GC85A (K260481) received a 510(k) decision of Substantially Equivalent on August 27, 2026, 195 days after the submission was received.
What is the product code of K260481?
The FDA product code is KPR – System, X-Ray, Stationary, a Class II (moderate risk) device regulated under 21 CFR 892.1680.