Msi 2002 Series Bed

FDA 510(k) K881027 · Med Service, Inc.

Substantially Equivalent

510(k) numberK881027

Submission

Device name
Msi 2002 Series Bed
Applicant
Med Service, Inc.
Batesville, MS, US
Received
March 10, 1988
Decision date
May 26, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K982783Vail 1000 Enclosed BedFNL · Traditional Vail Products, Inc.10/05/1998SE
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K974254Benefit B3--- SeriesFNL · Traditional M.C. Healthcare Products, Inc.12/16/1997SE
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

More from Hill-Rom, Inc.

510(k)DeviceDecision
K881961Msi Standard Bed Models: L1097-64 and L1085-64FNJ · Traditional 11/01/1988SE
K881960Msi Standard Bed Models L1098-84/L1098-74/L1085-74FNL · Traditional 11/01/1988SE
K881782Msi 4000 Series BedFNL · Traditional 07/12/1988SE
K881964Msi 3003 Series BedFNJ · Traditional 06/28/1988SE
K881963Msi 3002 Series BedFNL · Traditional 06/28/1988SE
K881962Msi 2005 Series BedFNJ · Traditional 06/03/1988SE
K881965Msi 5000 Series BedFNL · Traditional 05/31/1988SE
K873291Msi 9000 Series BedFNL · Traditional 12/30/1987SE

Questions and answers

When was Msi 2002 Series Bed cleared by the FDA?

Msi 2002 Series Bed (K881027) received a 510(k) decision of Substantially Equivalent on May 26, 1988, 77 days after the submission was received.

What is the product code of K881027?

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