Hilo Tables, Type CH-4, CH-8, FW-6, FW-5, FW-2, Al

FDA 510(k) K850873 · Ketronic, Inc.

Substantially Equivalent

510(k) numberK850873

Submission

Device name
Hilo Tables, Type CH-4, CH-8, FW-6, FW-5, FW-2, Al
Applicant
Ketronic, Inc.
The Netherlands, NL
Received
March 1, 1985
Decision date
June 12, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
INO – Chair, Positioning, Electric
Device class
Class II (moderate risk)
Regulation
21 CFR 890.3110
Specialty
Physical Medicine

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More from Winco, Inc.

510(k)DeviceDecision
K850877Monolift MPE2, Platform, Chair, Fully Futo PlatforILK · Traditional 06/12/1985SE
K850870Medifette Ergometer · Traditional 06/12/1985SE
K850869Mfe Couch ErgometerISD · Traditional 06/12/1985SE
K850868Mfe Cardiac Stress System · Traditional 06/12/1985SE
K850872Phyaction 300, 360, 370, 390 & 391 Elec-Muscle-Sti · Traditional 06/06/1985SN
K850871Tredband Type I, It, II & III - TreadmillsBXB · Traditional 06/05/1985SE
K850876Ligtvoet L80.2 Lightfoot L80.2 Power WheelchairITI · Traditional 05/16/1985SE
K850875Action-Wheels & Play Wheels · Traditional 05/16/1985SE
K843288Ketronic Medax - NIYX · Traditional 11/08/1984SE

Questions and answers

When was Hilo Tables, Type CH-4, CH-8, FW-6, FW-5, FW-2, Al cleared by the FDA?

Hilo Tables, Type CH-4, CH-8, FW-6, FW-5, FW-2, Al (K850873) received a 510(k) decision of Substantially Equivalent on June 12, 1985, 103 days after the submission was received.

What is the product code of K850873?

The FDA product code is INO – Chair, Positioning, Electric, a Class II (moderate risk) device regulated under 21 CFR 890.3110.