A-Bec 18

FDA 510(k) K865002 · A-Bec Mobility, Inc.

Substantially Equivalent

510(k) numberK865002

Submission

Device name
A-Bec 18
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

No product code recorded.

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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
K865005A-Bec 41ITI · Traditional 02/06/1987SE
K865004A-Bec 40 Power WheelchairITI · Traditional 02/06/1987SE
K865003A-Bec 46ITI · Traditional 02/06/1987SE

Questions and answers

When was A-Bec 18 cleared by the FDA?

A-Bec 18 (K865002) received a 510(k) decision of Substantially Equivalent on February 6, 1987, 46 days after the submission was received.