Xma 325 (X-Ray Generator)
FDA 510(k) K850117 · Summit Industries, Inc.
510(k) numberK850117
Submission
- Device name
- Xma 325 (X-Ray Generator)
- Applicant
- Summit Industries, Inc.
Chicago, IL, US - Received
- January 14, 1985
- Decision date
- April 9, 1985
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Other 510(k)s with product code IZO
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K954666 | MPH50, MPH65, and MPH80IZO · Traditional | GE Medical Systems | 11/24/1995SE |
| K953582 | HFX350, 30KW, 300MA, 1 or 3 Phase Radiographic & Fluoroscopic X-Ray GeneratorIZO · Traditional | Varian Canada, Inc. | 09/26/1995SE |
| K953831 | N 800 HFIZO · Traditional | Nucletron-Oldelft Corp. | 09/08/1995SE |
| K952822 | Shimadzu X-Ray High Viltage Generator AHD150GIZO · Traditional | Shimadzu Corp. | 07/12/1995SE |
| K952265 | Milestonw 350/450/550HF, PCX N350/450/550HF, Top-X 350/450/550HF Radiographic X-Ray…IZO · Traditional | Control-X, Inc. | 07/06/1995SE |
| K950883 | Polydoros SX 65 and 80IZO · Traditional | Siemens Medical Solutions USA, Inc. | 04/03/1995SE |
| K950694 | Compact-XIZO · Traditional | Electromed Intl., Ltd. | 03/31/1995SE |
| K950291 | Digital 625HFIZO · Traditional | Fischer Imaging Corp. | 03/23/1995SE |
| K950041 | Sii 360 AprIZO · Traditional | Scott Imaging Intl., Inc. | 03/21/1995SE |
| K950040 | Sii 525 AprIZO · Traditional | Scott Imaging Intl., Inc. | 03/21/1995SE |
More from Scott Imaging Intl., Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K173823 | Amrad Medical AAU Digital Radiography System; Amrad Medical AAU Plus Digital Radiography…KPR · Traditional | 02/09/2018SE |
| K153119 | Amrad Medical OTS Digital Radiography System, Amrad Medical DFMTS Digital Radiography…KPR · Traditional | 03/14/2016SE |
| K874908 | C900 X-Ray Film ProcessorIXW · Traditional | 02/12/1988SE |
| K874687 | Colli-Matetm Model No. B800IZX · Traditional | 12/30/1987SE |
| K851440 | Rdiographic Wall Holder or Film ReceptorIXY · Traditional | 06/05/1985SE |
| K850198 | Floor to Wall or Floor to Ceiling Tubestand;RadiogIYB · Traditional | 05/14/1985SE |
| K850118 | Xma Integrated TableIXQ · Traditional | 04/09/1985SE |
Questions and answers
When was Xma 325 (X-Ray Generator) cleared by the FDA?
Xma 325 (X-Ray Generator) (K850117) received a 510(k) decision of Substantially Equivalent on April 9, 1985, 85 days after the submission was received.
What is the product code of K850117?
The FDA product code is IZO – Generator, High-Voltage, X-Ray, Diagnostic, a Class I (low risk) device regulated under 21 CFR 892.1700.