A-Bec 41

FDA 510(k) K865005 · A-Bec Mobility, Inc.

Substantially Equivalent

510(k) numberK865005

Submission

Device name
A-Bec 41
Applicant
A-Bec Mobility, Inc.
Torrance, CA, US
Received
December 22, 1986
Decision date
February 6, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
ITI – Wheelchair, Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 890.3860
Specialty
Physical Medicine

A powered wheelchair is a battery-operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. FDA interprets “mobility to persons restricted to a sitting position” to mean the device type is intended to provide mobility to individuals who have mobility impairments and require an assistive device for mobility. NOTE: This type…

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More from Whill, Inc.

510(k)DeviceDecision
K880425Sterling (Motorized Vehicle)INI · Traditional 02/16/1988SE
K880424Scoota Bug (Motorized Vehicle)INI · Traditional 02/16/1988SE
K880423Targa (Wheelchair)ITI · Traditional 02/16/1988SE
K865009A-Bec 47ITI · Traditional 02/06/1987SE
K865008A-Bec 17ITI · Traditional 02/06/1987SE
K865007A-Bec 15ITI · Traditional 02/06/1987SE
K865006A-Bec 14ITI · Traditional 02/06/1987SE
K865004A-Bec 40 Power WheelchairITI · Traditional 02/06/1987SE
K865003A-Bec 46ITI · Traditional 02/06/1987SE
K865002A-Bec 18 · Traditional 02/06/1987SE

Questions and answers

When was A-Bec 41 cleared by the FDA?

A-Bec 41 (K865005) received a 510(k) decision of Substantially Equivalent on February 6, 1987, 46 days after the submission was received.

What is the product code of K865005?

The FDA product code is ITI – Wheelchair, Powered, a Class II (moderate risk) device regulated under 21 CFR 890.3860.