Sween Universal Bed Rail Pads

FDA 510(k) K810846 · Sween Corp.

Substantially Equivalent

510(k) numberK810846

Submission

Device name
Sween Universal Bed Rail Pads
Applicant
Sween Corp.
Mchenry, IL, US
Received
March 27, 1981
Decision date
April 17, 1981
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FNJ – Bed, Manual
Device class
Class I (low risk)
Regulation
21 CFR 880.5120
Specialty
General Hospital

Other 510(k)s with product code FNJ

510(k)DeviceApplicantDecision
K934298King KribFNJ · Traditional Noritage, Inc.01/26/1994SE
K892877Cradle, Hospital Bed ClothingFNJ · Traditional Warsaw Orthopedic, Inc.06/15/1989SE
K885241Bed, Adjustable, Hospital, Folding, Field, W/O MatFNJ · Traditional King Mfg. Co.02/24/1989SE
K884542Sic 3999 Folding Adjustable Hospital BedFNJ · Traditional Commercial Products & Engineering Co.11/21/1988SE
K881725Envirotent (Bed)FNJ · Traditional Envirotents, Inc.11/08/1988SE
K881961Msi Standard Bed Models: L1097-64 and L1085-64FNJ · Traditional Med Service, Inc.11/01/1988SE
K881964Msi 3003 Series BedFNJ · Traditional Med Service, Inc.06/28/1988SE
K881962Msi 2005 Series BedFNJ · Traditional Med Service, Inc.06/03/1988SE
K881043Folding Hospital Cot NSN 6530-00-299-8517FNJ · Traditional Junkin Safety Appliance Co., Inc.04/12/1988SE
K870166Platform Mattress W/Disposable Bedpan BagFNJ · Traditional George C. Kuhn03/13/1987SE

More from George C. Kuhn

510(k)DeviceDecision
K926389Sween Wound Care-Collagen Wound DressingMGQ · Traditional 07/08/1993SE
K912506Critic-Aid Wound DressingKMF · Traditional 03/02/1992SE
K840723Sween-A-Peel Peristomal WafersEXB · Traditional 05/07/1984SE

Questions and answers

When was Sween Universal Bed Rail Pads cleared by the FDA?

Sween Universal Bed Rail Pads (K810846) received a 510(k) decision of Substantially Equivalent on April 17, 1981, 21 days after the submission was received.

What is the product code of K810846?

The FDA product code is FNJ – Bed, Manual, a Class I (low risk) device regulated under 21 CFR 880.5120.