Comfortex Wheelchair Cushion

FDA 510(k) K855181 · Comfortex, Inc.

Substantially Equivalent

510(k) numberK855181

Submission

Device name
Comfortex Wheelchair Cushion
Applicant
Comfortex, Inc.
Winona, MN, US
Received
December 26, 1985
Decision date
January 13, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KNN – Components, Wheelchair
Device class
Class I (low risk)
Regulation
21 CFR 890.3920
Specialty
Physical Medicine

Other 510(k)s with product code KNN

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K211919KISS Dynamic Back Support, KISS Dynamic Solid Drop SeatKNN · Traditional Kinetic Innovative Seating System, LLC03/04/2022SE
K942311Dynasty U1-33 AgmKNN · Traditional Foley & Lardner11/07/1994SE
K942310Dynasty GC 12550 (Gell/Cell)KNN · Traditional Foley & Lardner11/07/1994SE
K942309Dynasty U1-31 (Gell/Cell)KNN · Traditional Foley & Lardner11/07/1994SE
K942308Dynasty GC 12400 (Gell/Cell)KNN · Traditional Foley & Lardner11/07/1994SE
K942312Alden Lineage Wheelchair CushionKNN · Traditional Lewis W. Ward05/26/1994SE
K942260Alden Wheelchair CushionKNN · Traditional Ward and Assoc.05/26/1994SE
K933051Zero Gravity Wheelchair Components, ModificationKNN · Traditional General Components Intl., Inc.10/12/1993SE
K925980PMKNN · Traditional Pathfinder Intl. Corp.03/24/1993SE
K923942Rhombo Medical Rhombo-FillKNN · Traditional International Medical Products, Inc.03/24/1993SE

More from International Medical Products, Inc.

510(k)DeviceDecision
K860037Suspender Orthopedic Suspension DeviceHST · Traditional 01/21/1986SE
K855179Transfer-Trax (TM) Splint TractionHST · Traditional 01/21/1986SE
K854270Murphy Adjustable SplintKQZ · Traditional 12/09/1985SE

Questions and answers

When was Comfortex Wheelchair Cushion cleared by the FDA?

Comfortex Wheelchair Cushion (K855181) received a 510(k) decision of Substantially Equivalent on January 13, 1986, 18 days after the submission was received.

What is the product code of K855181?

The FDA product code is KNN – Components, Wheelchair, a Class I (low risk) device regulated under 21 CFR 890.3920.