Heel Protector
FDA 510(k) K771633 · Medical Restraints, Inc.
510(k) numberK771633
Submission
- Device name
- Heel Protector
- Applicant
- Medical Restraints, Inc.
Mchenry, IL, US - Received
- August 26, 1977
- Decision date
- September 12, 1977
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- FMP – Protector, Skin Pressure
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 880.6450
- Specialty
- General Hospital
Other 510(k)s with product code FMP
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K150243 | Invictus Medical GelShieldFMP · Traditional | Invictus Medical, Inc. | 05/01/2015SE |
| K951325 | Comfeel Plus Pressure Relief DressingFMP · Traditional | Richard Hamer Assoc., Inc. | 07/31/1995SE |
| K934731 | Medsurg Sterile Imaging ProductsFMP · Traditional | Medsurg Industries, Inc. | 03/28/1994SE |
| K820584 | Decubicare Pads & AccessoriesFMP · Traditional | Abco Dealers, Inc. | 03/25/1982SE |
| K812344 | Heel or Elbow ProtectorFMP · Traditional | Fred Sammons, Inc. | 09/11/1981SE |
| K811184 | Spenco Dermal PadsFMP · Traditional | Spenco Medical Corp. | 05/20/1981SE |
| K802829 | Scanlan Vascu-StattFMP · Traditional | Scanlan Intl., Inc. | 01/15/1981SE |
| K802185 | Arterial Blood Sampling KitFMP · Traditional | Current Technologies, Inc. | 10/10/1980SE |
| K801694 | Flotation Pad for Operating TableFMP · Traditional | Action Products, Inc. | 08/27/1980SE |
| K801195 | Dermalex or Natrawool Skin Pressure ProtFMP · Traditional | Stock Wild & Co. | 06/09/1980SE |
More from Stock Wild & Co.
| 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 |
| K771632 | Finger Mitt RestraintFMQ · Traditional | 09/28/1977SE |
| K771676 | Foot Drop BootIQI · Traditional | 09/20/1977SE |
| K771631 | Wheelchair Safety BeltKNN · Traditional | 09/12/1977SE |
Questions and answers
When was Heel Protector cleared by the FDA?
Heel Protector (K771633) received a 510(k) decision of Substantially Equivalent on September 12, 1977, 17 days after the submission was received.
What is the product code of K771633?
The FDA product code is FMP – Protector, Skin Pressure, a Class I (low risk) device regulated under 21 CFR 880.6450.