Wearable Device ; Cradle ; Small Strap, Medium Strap, Large Strap ; Multiple Device Charger ; Hospital Starter Package

FDA 510(k) K182543 · Snap40, Ltd.

Substantially Equivalent

510(k) numberK182543

Submission

Device name
Wearable Device ; Cradle ; Small Strap, Medium Strap, Large Strap ; Multiple Device Charger ; Hospital Starter Package
Applicant
Snap40, Ltd.
Edinburgh, GB
Received
September 17, 2018
Decision date
November 14, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

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

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K261287Digistat CareMSX · Traditional Ascom Ums Srl Unipersonale09/12/2026SE
K260211Dashboard (P007000)MSX · Traditional Hill-Rom, Inc.08/13/2026SE
K261367Corsano CardioWatch 287-2 SystemMSX · Traditional Corsano Health B.V.07/26/2026SE
K253654IntelliVue Measurement Rack 6000 (867317)MSX · Traditional Philips Medizin Systeme Böblingen GmbH03/30/2026SE
K243270TigerConnect Alarm ManagementMSX · Traditional Tigerconnect09/30/2025SE
K242728BeneVision Central Monitoring SystemMSX · Traditional Shenzhen Mindray Bio-Medical Electronics Co., Ltd.07/31/2025SE
K242750Central StationMSX · Traditional Nihon Kohden Digital Health Solutions, LLC06/05/2025SE
K242842ANNE View, Central HubMSX · Traditional Sibel Health, Inc.01/08/2025SE
K241397HinscopeMSX · Traditional Hinlab Sas11/14/2024SE
K233834Infinity Gateway SuiteMSX · Traditional Draeger Medical Systems, Inc.07/12/2024SE

Questions and answers

When was Wearable Device ; Cradle ; Small Strap, Medium Strap, Large Strap ; Multiple Device Charger ; Hospital Starter Package cleared by the FDA?

Wearable Device ; Cradle ; Small Strap, Medium Strap, Large Strap ; Multiple Device Charger ; Hospital Starter Package (K182543) received a 510(k) decision of Substantially Equivalent on November 14, 2018, 58 days after the submission was received.

What is the product code of K182543?

The FDA product code is MSX – System, Network And Communication, Physiological Monitors, a Class II (moderate risk) device regulated under 21 CFR 870.2300.