Kaye Model Kiao Pelvic/Thigh Stabilizer

FDA 510(k) K923095 · Kaye Products, Inc.

Substantially Equivalent

510(k) numberK923095

Submission

Device name
Kaye Model Kiao Pelvic/Thigh Stabilizer
Applicant
Kaye Products, Inc.
Hillsborough, NC, US
Received
June 25, 1992
Decision date
July 21, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
INN – Chair, Adjustable, Mechanical
Device class
Class I (low risk)
Regulation
21 CFR 890.3100
Specialty
Physical Medicine

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K922061Chair, Adjustable, MechanicalINN · Traditional Kaye Products, Inc.05/26/1992SE
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K904069Broda Nursing Care ChairINN · Traditional Broda Ent., Inc.09/17/1990SE
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More from Tri-S-Sales and Mfg.

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K885330Wheelchair, MechanicalIOR · Traditional 02/03/1989SE
K833869Child's WalkerITJ · Traditional 11/29/1983SE
K830560Exerciser, Passive, Non MeasuringION · Traditional 03/09/1983SE
K830466Bars, Parallel, ExerciseIOE · Traditional 03/09/1983SE
K820591Mechanical ChairLBE · Traditional 03/15/1982SE
K812399Chair, Adjustable, MechanicalINN · Traditional 09/14/1981SE
K812319Therapy BenchIOD · Traditional 08/31/1981SE
K810609Pediatric Position HolderFRP · Traditional 03/20/1981SE

Questions and answers

When was Kaye Model Kiao Pelvic/Thigh Stabilizer cleared by the FDA?

Kaye Model Kiao Pelvic/Thigh Stabilizer (K923095) received a 510(k) decision of Substantially Equivalent on July 21, 1992, 26 days after the submission was received.

What is the product code of K923095?

The FDA product code is INN – Chair, Adjustable, Mechanical, a Class I (low risk) device regulated under 21 CFR 890.3100.