# K963436: Restraint Accessories

- Pathway: 510(k) (Traditional)
- Applicant: J. T. Posey Co.
- Decided: Nov 22, 1996 after 84 days
- Product code: FMQ (Restraint, Protective)
- Device class: 1
- Regulation: 21 CFR 880.6760
- Recalls of this device: 22 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Protective Restraints: named in the summary without a submission number

## Recalls of this device
- Apr 20, 2009 · Not classified · Z-2268-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2272-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2257-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2254-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2256-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2274-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2260-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2267-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2261-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2264-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2263-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2269-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2265-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2275-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2255-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2259-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2273-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2266-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2271-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2270-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2258-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten
- Apr 20, 2009 · Not classified · Z-2262-2009: Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the exten

## Indications for use
The devices included in this 510(k) submission facilitate attachment of protective restraint devices to vehicles. These devices provide anchor points for tying quick release knots and/or adapts protective restraints with quick release buckles. The products are then secured to the bed, geriatric chair, or wheelchair via the accessory device. The accessory devices attach directly to the vehicle. These products are facilitate attachment of devices that are intended to hinder egress or aid in positioning of a patient in a wheelchair, hospital bed, geriatric chair, or gumey.

Source page: https://510kreport.com/device/K963436
Methodology: https://510kreport.com/methodology