Technomed Generator, Radiographic, 3 Phase
FDA 510(k) K827126 · Tecnomed, Inc.
510(k) numberK827126
Submission
- Device name
- Technomed Generator, Radiographic, 3 Phase
- Applicant
- Tecnomed, Inc.
Richmond, VA, US - Received
- February 4, 1982
- Decision date
- March 5, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Tecnomed, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K892226 | Tec 6340 90/15 Radiographic/Fluoroscopic TableIXR · Traditional | 04/26/1989SE |
| K854203 | Tec 2720 Mamex DC MagIZH · Traditional | 03/06/1986SE |
| K827124 | Ralco Collimator, Automatic, Radiographic · Traditional | 03/05/1982SE |
| K820307 | Tecnomed Generator, Radiograph., 3 PhaseIZO · Traditional | 03/05/1982SE |
| K820306 | Ralco Collimator, Automatic RadiographicKPW · Traditional | 03/05/1982SE |
| K827125 | Ralco Collimators, Manual, Radiographic · Traditional | 03/04/1982SE |
| K820305 | Ralco Collimators, Manual RadiographicKPW · Traditional | 03/04/1982SE |
| K811197 | Superix 120IZF · Traditional | 06/09/1981SE |
| K811196 | Allmec 90/15KXJ · Traditional | 06/09/1981SE |
| K811195 | ArgostatIYB · Traditional | 06/09/1981SE |
Questions and answers
When was Technomed Generator, Radiographic, 3 Phase cleared by the FDA?
Technomed Generator, Radiographic, 3 Phase (K827126) received a 510(k) decision of Substantially Equivalent on March 5, 1982, 29 days after the submission was received.