Protective Restraint - Belts
FDA 510(k) K963490 · Smith and Nephew Donjoy, Inc.
510(k) numberK963490
Submission
- Device name
- Protective Restraint - Belts
- Applicant
- Smith and Nephew Donjoy, Inc.
Vista, CA, US - Received
- September 3, 1996
- Decision date
- November 12, 1996
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FMQ – Restraint, Protective
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 880.6760
- Specialty
- General Hospital
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|---|---|---|---|
| K110377 | Protective RestraintFMQ · Traditional | Medi-Tech Intl. Corp. | 04/25/2011SE |
| K081264 | Statstrap Neonatal Incubator Safety Strap, Models SS-001, SS-002FMQ · Traditional | Children'S Health First, Inc. | 02/13/2009SE |
| K080448 | Centurion Protective Restraint, SCR SeriesFMQ · Traditional | Tri-State Hospital Supply Corp. | 08/28/2008SE |
| K013239 | Comfortcare Compression Support with Magnets Comfortcare Magnetic InsolesFMQ · Traditional | Med Gen, Inc. | 11/20/2001SE |
| K010818 | Infant Limb Holder, Models 306080 & 306081FMQ · Traditional | Skil-Care Corp. | 05/24/2001SE |
| K010644 | Cinch-Type Disposable Limb Holders, Model 912025FMQ · Traditional | Skil-Care Corp. | 05/18/2001SE |
| K991591 | Biothane Patient RestraintFMQ · Traditional | Bioplastics | 07/29/1999SE |
| K982178 | Vagabond Soft Restraint SystemFMQ · Traditional | Emergent Innovations, Ltd. | 01/26/1999SE |
| K980640 | Heelbo Waist and Chest VestFMQ · Traditional | Heelbo, Inc. | 05/01/1998SE |
| K972446 | Pedo Cush Pedo CuddleFMQ · Traditional | Cavity Free Kids, Inc. | 11/13/1997SE |
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| 510(k) | Device | Decision |
|---|---|---|
| K970051 | Musclesense II Clinical Electromyography DeviceHCC · Traditional | 07/10/1997SE |
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| K963489 | Wheel Chair AccessoryFMQ · Traditional | 11/12/1996SE |
| K962462 | Musclemax Plus Electrical Muscle StimulatorIPF · Traditional | 09/23/1996SE |
| K955057 | Model 1100 Cold Therapy DeviceILO · Traditional | 03/08/1996SN |
| K951350 | Musclesense Electromyography DeviceHCC · Traditional | 06/23/1995SE |
| K945687 | Rounded Cannulated Inside-Out (Rci) Acl ScrewHWC · Traditional | 06/22/1995SN |
| K946313 | Tibial Routers, Femoral Routers and Tube Graft SizerHRX · Traditional | 03/17/1995SE |
| K945236 | Aims Cannulated Acl Screw (7MM Diameter)HWC · Traditional | 02/03/1995SE |
| K932592 | Brace NeutralizerGZJ · Traditional | 03/18/1994SE |
Questions and answers
When was Protective Restraint - Belts cleared by the FDA?
Protective Restraint - Belts (K963490) received a 510(k) decision of Substantially Equivalent on November 12, 1996, 70 days after the submission was received.
What is the product code of K963490?
The FDA product code is FMQ – Restraint, Protective, a Class I (low risk) device regulated under 21 CFR 880.6760.