Finger Mitt Restraint
FDA 510(k) K771632 · Medical Restraints, Inc.
510(k) numberK771632
Submission
- Device name
- Finger Mitt Restraint
- Applicant
- Medical Restraints, Inc.
Mchenry, IL, US - Received
- August 26, 1977
- Decision date
- September 28, 1977
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- FMQ – Restraint, Protective
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 880.6760
- Specialty
- General Hospital
Other 510(k)s with product code FMQ
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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 |
More from Cavity Free Kids, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K771636 | Body RestraintFMQ · Traditional | 09/30/1977SE |
| K771630 | Limb RestraintFMQ · Traditional | 09/30/1977SE |
| K771629 | Hand RestraintFMQ · Traditional | 09/30/1977SE |
| K771715 | Pelvic Wheelchair RestraintFMQ · Traditional | 09/28/1977SE |
| K771635 | Foot ElevatorFMQ · Traditional | 09/28/1977SE |
| K771634 | Vest RestraintFMQ · Traditional | 09/28/1977SE |
| K771676 | Foot Drop BootIQI · Traditional | 09/20/1977SE |
| K771633 | Heel ProtectorFMP · Traditional | 09/12/1977SE |
| K771631 | Wheelchair Safety BeltKNN · Traditional | 09/12/1977SE |
Questions and answers
When was Finger Mitt Restraint cleared by the FDA?
Finger Mitt Restraint (K771632) received a 510(k) decision of Substantially Equivalent on September 28, 1977, 33 days after the submission was received.
What is the product code of K771632?
The FDA product code is FMQ – Restraint, Protective, a Class I (low risk) device regulated under 21 CFR 880.6760.