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Medical Disposable Bedding

FDA 510(k)

Class II (US FDA 510(k))

510(k) K924420

by Hill-Rom, Inc.

Identifiers

510(k) Number
K924420 FDA 510(k)
FDA Product Code
KNC FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 884.4900 FDA 510(k)
Regulation Number
884.4900 FDA 510(k)
Advisory Committee
Obstetrics/Gynecology FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Medical Disposable Bedding is a device classified as a Table, Obstetric (And Accessories) under regulation number 884.4900. It is intended for use in obstetrics and gynecology settings.

The device is supplied as a disposable product and received FDA 510(k) clearance (K924420) on December 10, 1993, from Hill-Rom, Inc. It is manufactured in the United States and registered under the listed FEI and registration numbers.

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: MEDICAL DISPOSABLE BEDDING (K924420) — FDA 510(k) | Innolitics, Medical Disposable Bedding 510 (k) FDA Premarket Notification K924420 ..., Hill-Rom - Wikipedia

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Hill-Rom, Inc.

Sources (1)

  • FDA 510(k) K924420 24 fields · synced Sep 24, 2026