The Nomos Crane
FDA 510(k) K941927 · Nomos Corp.
510(k) numberK941927
Submission
- Device name
- The Nomos Crane
- Applicant
- Nomos Corp.
Sewickley, PA, US - Received
- April 20, 1994
- Decision date
- February 9, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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| K122413 | Patient Positioning SystemJAI · Traditional | Forte Automation Systems, Inc. | 09/13/2012SE |
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More from Medical Intelligence Medizintechnik GmbH
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| K042875 | NavigatorIYE · Traditional | 07/01/2005SE |
| K032209 | Nomos Corvus 5.0MMUJ · Special | 08/21/2003SE |
| K013036 | Nomos Motorized Crane IIJAI · Traditional | 12/07/2001SE |
| K993675 | Peregrine Radiation Therapy Dose Calculation SystemMUJ · Traditional | 09/05/2000SE |
| K993359 | Raptor Treatment Planning SystemIYE · Traditional | 12/21/1999SE |
| K991966 | The Nomos Chane IIIYE · Traditional | 09/03/1999SE |
| K981424 | Nomos Bat Ultrasound Localization and Positioning SystemIYE · Traditional | 07/17/1998SE |
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Questions and answers
When was The Nomos Crane cleared by the FDA?
The Nomos Crane (K941927) received a 510(k) decision of Substantially Equivalent on February 9, 1995, 295 days after the submission was received.
What is the product code of K941927?
The FDA product code is JAI – Couch, Radiation Therapy, Powered, a Class II (moderate risk) device regulated under 21 CFR 892.5770.