Walking Aid
FDA 510(k) K770608 · Will Ross Co.
510(k) numberK770608
Submission
- Device name
- Walking Aid
- Applicant
- Will Ross Co.
Mchenry, IL, US - Received
- March 31, 1977
- Decision date
- April 8, 1977
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- ITJ – Walker, Mechanical
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 890.3825
- Specialty
- Physical Medicine
Other 510(k)s with product code ITJ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K833869 | Child's WalkerITJ · Traditional | Kaye Products, Inc. | 11/29/1983SE |
| K833195 | Umbrella WalkerITJ · Traditional | Convaid Products, Inc. | 10/27/1983SE |
| K830784 | Walk N RollITJ · Traditional | Meta-Morris | 05/25/1983SE |
| K830848 | Resi-WalkerITJ · Traditional | Lic-Orthion | 04/05/1983SE |
| K823105 | Resi-WalkerITJ · Traditional | Orthion Corp. | 11/05/1982SE |
| K821404 | Light Weight Aluminum WalkerITJ · Traditional | Manuco Manufacturing Co., Inc. | 05/21/1982SE |
| K820711 | Walk-A-CycleITJ · Traditional | Walk-A-Cycle Division | 04/08/1982SE |
| K811485 | Walker/Crutch BagITJ · Traditional | Fred Sammons, Inc. | 06/16/1981SE |
| K792064 | Delta Rolling Self-Licking WalkerITJ · Traditional | Staricat, Inc. | 10/30/1979SE |
| K790529 | Walking AidITJ · Traditional | Maddak, Inc. | 04/03/1979SE |
More from Maddak, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K780850 | Searle Neonatal Oxygen ProbeCCE · Traditional | 08/23/1978SE |
| K771561 | Dover Urine MeterEXR · Traditional | 09/07/1977SE |
| K771132 | Kenwood Biological Steoiliz. IndicatorFRC · Traditional | 07/14/1977SE |
| K770612 | Splint, BohlerIQI · Traditional | 04/08/1977SE |
| K770611 | Parallel BarsIOE · Traditional | 04/08/1977SE |
| K770610 | Table, Treatment & Traction, Hi-LoITH · Traditional | 04/08/1977SE |
| K770609 | Table, Massage & Treatmhnt, Fixed HeightINT · Traditional | 04/08/1977SE |
| K770607 | Traction HarnessILZ · Traditional | 04/08/1977SE |
| K770509 | Table, Massage and TreatmentINT · Traditional | 04/05/1977SE |
| K770399 | Valve for Closed Sys. Urinary DrainageKNX · Traditional | 03/09/1977SE |
Questions and answers
When was Walking Aid cleared by the FDA?
Walking Aid (K770608) received a 510(k) decision of Substantially Equivalent on April 8, 1977, 8 days after the submission was received.
What is the product code of K770608?
The FDA product code is ITJ – Walker, Mechanical, a Class I (low risk) device regulated under 21 CFR 890.3825.