N 800 HF
FDA 510(k) K950037 · Oldelft Corp. of America
510(k) numberK950037
Submission
- Device name
- N 800 HF
- Applicant
- Oldelft Corp. of America
Fairfax, VA, US - Received
- January 4, 1995
- Decision date
- February 15, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
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|---|---|---|---|
| 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 |
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| K946128 | Simulix-HpKPQ · Traditional | 05/12/1995SE |
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| K923584 | Therapax DXT 300 Series 3JAD · Traditional | 01/15/1993SE |
| K914784 | Papillion ProctoscopeKQA · Traditional | 06/05/1992SE |
| K912466 | Oldelft Simulix-McKPQ · Traditional | 06/28/1991SE |
| K892659 | ElectrodelcaIZG · Traditional | 11/21/1989SE |
Questions and answers
When was N 800 HF cleared by the FDA?
N 800 HF (K950037) received a 510(k) decision of Substantially Equivalent on February 15, 1995, 42 days after the submission was received.
What is the product code of K950037?
The FDA product code is IZO – Generator, High-Voltage, X-Ray, Diagnostic, a Class I (low risk) device regulated under 21 CFR 892.1700.