The Genesis Bed From Hill-Rom, Model 355 Series

FDA 510(k) K914309 · Hill-Rom, Inc.

Substantially Equivalent

510(k) numberK914309

Submission

Device name
The Genesis Bed From Hill-Rom, Model 355 Series
Applicant
Hill-Rom, Inc.
Batesville, TN, US
Received
September 25, 1991
Decision date
April 20, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
HDD – Table, Obstetrical, Ac-Powered (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 884.4900
Specialty
Obstetrics/Gynecology

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K875123OrcepadHDD · Traditional Alton Dean Medical, Inc.06/21/1988SE
K874610Adel Model 2100 Birthing BedHDD · Traditional Adel Medical , Ltd.01/21/1988SE
K810886Adel Medical Birthing Bed, #LD-500HDD · Traditional Adel Medical , Ltd.04/23/1981SE
K771942Tilt 10, Catalog #S-2600HDD · Traditional Affiliated Hospital Products, Inc.10/27/1977SE
K770438Cart, ProceduresHDD · Traditional I E Industries07/01/1977SE

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Questions and answers

When was The Genesis Bed From Hill-Rom, Model 355 Series cleared by the FDA?

The Genesis Bed From Hill-Rom, Model 355 Series (K914309) received a 510(k) decision of Substantially Equivalent on April 20, 1992, 208 days after the submission was received.

What is the product code of K914309?

The FDA product code is HDD – Table, Obstetrical, Ac-Powered (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 884.4900.