Berkeley Fork

FDA 510(k) K823876 · Berkeley Electric Wheelchair Co.

Substantially Equivalent

510(k) numberK823876

Submission

Device name
Berkeley Fork
Applicant
Berkeley Electric Wheelchair Co.
Mchenry, IL, US
Received
December 28, 1982
Decision date
January 14, 1983
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

510(k)DeviceApplicantDecision
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
K823085Berkeley ChairITI · Traditional 01/21/1983SE
K823877Berkeley HarnessKNN · Traditional 01/14/1983SE
K823875Chain KitKNN · Traditional 01/14/1983SE
K823874Berkeley BrakeKNN · Traditional 01/14/1983SE
K823873Chain SilencerKNN · Traditional 01/14/1983SE

Questions and answers

When was Berkeley Fork cleared by the FDA?

Berkeley Fork (K823876) received a 510(k) decision of Substantially Equivalent on January 14, 1983, 17 days after the submission was received.

What is the product code of K823876?

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