Tourniquet Test Gage
FDA 510(k) K790247 · Orthopedic Equipment Co., Inc.
510(k) numberK790247
Submission
- Device name
- Tourniquet Test Gage
- Applicant
- Orthopedic Equipment Co., Inc.
Mchenry, IL, US - Received
- February 6, 1979
- Decision date
- February 26, 1979
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Orthopedic Equipment Co., Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K834035 | Universal Self-Aligning Acetabular ComJDI · Traditional | 06/19/1984SE |
| K841189 | Oec/Rezaian Spinal FixatorKWQ · Traditional | 05/16/1984SE |
| K800530 | Schlein Tri-Surface AnkleHSN · Traditional | 04/02/1980SE |
| K781445 | SpreaderGAD · Traditional | 09/27/1979SE |
| K790209 | Filter System, Altner DisposableGAZ · Traditional | 02/26/1979SE |
| K781451 | Flat WrenchHXS · Traditional | 09/27/1978SE |
| K781450 | DriversGFC · Traditional | 09/27/1978SE |
| K781449 | Harrington Spinal ElevatorGEG · Traditional | 09/27/1978SE |
| K781448 | Harrington Hook ClampGEN · Traditional | 09/27/1978SE |
| K781447 | Threaded Rod ClampGEN · Traditional | 09/27/1978SE |
Questions and answers
When was Tourniquet Test Gage cleared by the FDA?
Tourniquet Test Gage (K790247) received a 510(k) decision of Substantially Equivalent on February 26, 1979, 20 days after the submission was received.