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Via Stretcher (P1300 - P1303)

FDA 510(k)EUDAMED

Class II (US FDA 510(k))

510(k) K922808

by Hill-Rom, Inc.

Identifiers

510(k) Number
K922808 FDA 510(k)
FDA Product Code
FPO FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 880.6910 FDA 510(k)
Regulation Number
880.6910 FDA 510(k)
Advisory Committee
General Hospital FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

The Via Stretcher (P1300 - P1303) is a wheeled stretcher designed for patient transport and handling in clinical settings. It is classified as a Class II medical device under FDA regulations, intended for use in general hospital environments to safely move patients between care locations while maintaining stability and comfort.

This device is supplied as a reusable stretcher, intended for use in hospital settings. It is regulated under FDA 510(k) clearance (K922808) and the MDR (Medical Device Regulation) framework, with a product code of FPO. Multiple model variants (P1300–P1303) are available, each adhering to the same regulatory and functional standards for patient transport.

This description and any FAQs above were generated automatically from registry data and have not been verified by the manufacturer or by deviCERTS. Always check the official registry entry and the manufacturer's instructions for use before relying on them. Sources consulted: HILL-ROM VIA STRETCHER (P1300 - P1303) - Innolitics, PDF K922808 - Hill-rom Via Stretcher (P1300 - P1303), HILL-ROM VIA STRETCHER (P1300 - P1303) 510(k) K922808 - fda.report

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

MDR

United States Active

FDA_510K

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Manufacturer

Manufacturer
Hill-Rom, Inc.

Sources (2)

  • FDA 510(k) K922808 24 fields · synced Oct 6, 2026
  • EUDAMED 1 fields · synced May 19, 2026