iBed Wireless with iBed Mobile

FDA 510(k) K202964 · Stryker Corporation

Substantially Equivalent

510(k) numberK202964

Submission

Device name
iBed Wireless with iBed Mobile
Applicant
Stryker Corporation
Portage, MI, US
Received
September 30, 2020
Decision date
June 18, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FNL – Bed, Ac-Powered Adjustable Hospital
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5100
Specialty
General Hospital

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K974296Model 720 Series Full/Semi Electric Bed 1120 Full Electric BedFNL · Traditional Invacare Corp.01/06/1998SE
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K972115Volker Hospital Bed, Model K960FNL · Traditional Volker Healthcare, Inc.08/29/1997SE
K971546Soma 900 Transport BedFNL · Traditional Nova Technologies, Inc.07/10/1997SE
K963622Vail 2000 Enclosed BedFNL · Traditional Vail Products, Inc.05/07/1997SE
K963589Vail 3000 Bed EnclosureFNL · Traditional Vail Products, Inc.04/21/1997SE
K962942TotalcareFNL · Traditional Hill-Rom, Inc.02/03/1997SE
K963701Soma Safe EnclosureFNL · Traditional Nova Technology Corp.01/24/1997SE

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Questions and answers

When was iBed Wireless with iBed Mobile cleared by the FDA?

iBed Wireless with iBed Mobile (K202964) received a 510(k) decision of Substantially Equivalent on June 18, 2021, 261 days after the submission was received.

What is the product code of K202964?

The FDA product code is FNL – Bed, Ac-Powered Adjustable Hospital, a Class II (moderate risk) device regulated under 21 CFR 880.5100.