Hinscope
FDA 510(k) K241397 · Hinlab Sas
510(k) numberK241397
Submission
- Device name
- Hinscope
- Applicant
- Hinlab Sas
Neuilly Sur Seine, FR - Received
- May 16, 2024
- Decision date
- November 14, 2024
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MSX – System, Network And Communication, Physiological Monitors
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.2300
- Specialty
- Cardiovascular
- Life-sustaining
- Yes
Other 510(k)s with product code MSX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261287 | Digistat CareMSX · Traditional | Ascom Ums Srl Unipersonale | 09/12/2026SE |
| K260211 | Dashboard (P007000)MSX · Traditional | Hill-Rom, Inc. | 08/13/2026SE |
| K261367 | Corsano CardioWatch 287-2 SystemMSX · Traditional | Corsano Health B.V. | 07/26/2026SE |
| K253654 | IntelliVue Measurement Rack 6000 (867317)MSX · Traditional | Philips Medizin Systeme Böblingen GmbH | 03/30/2026SE |
| K243270 | TigerConnect Alarm ManagementMSX · Traditional | Tigerconnect | 09/30/2025SE |
| K242728 | BeneVision Central Monitoring SystemMSX · Traditional | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | 07/31/2025SE |
| K242750 | Central StationMSX · Traditional | Nihon Kohden Digital Health Solutions, LLC | 06/05/2025SE |
| K242842 | ANNE View, Central HubMSX · Traditional | Sibel Health, Inc. | 01/08/2025SE |
| K233834 | Infinity Gateway SuiteMSX · Traditional | Draeger Medical Systems, Inc. | 07/12/2024SE |
| K233418 | Biofourmis Everion+ (G2)MSX · Traditional | Biofourmis Singapore Pte., Ltd. | 05/09/2024SE |
More from Biofourmis Singapore Pte., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K231531 | PediarityDQA · Traditional | 12/21/2023SE |
Questions and answers
When was Hinscope cleared by the FDA?
Hinscope (K241397) received a 510(k) decision of Substantially Equivalent on November 14, 2024, 182 days after the submission was received.
What is the product code of K241397?
The FDA product code is MSX – System, Network And Communication, Physiological Monitors, a Class II (moderate risk) device regulated under 21 CFR 870.2300.