Kodak Digital Science Medical Modality Acquisition Unit
FDA 510(k) K961739 · Kodak Health Imaging Systems, Inc.
510(k) numberK961739
Submission
- Device name
- Kodak Digital Science Medical Modality Acquisition Unit
- Applicant
- Kodak Health Imaging Systems, Inc.
Dallas, TX, US - Received
- May 3, 1996
- Decision date
- November 14, 1996
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Other 510(k)s with product code LLZ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262060 | 3D-RD-SLLZ · Traditional | Radiopharmaceutical Imaging & Dosimetry, LLC | 09/04/2026SE |
| K261500 | KBA3D (v2.4.0)LLZ · Traditional | S.M.A.I.O | 08/17/2026SE |
| K262449 | AdvaViewLLZ · Special | Advahealth Solutions, LLC | 08/14/2026SE |
| K261916 | NeuroQuant PETLLZ · Traditional | Cortechs Labs, Inc. | 08/12/2026SE |
| K260936 | RadioViewAILLZ · Traditional | Neurocareai, Inc. (Dba Savelife.Ai) | 07/31/2026SE |
| K260588 | Cleerly LABSLLZ · Traditional | Cleerly, Inc. | 07/29/2026SE |
| K262462 | TheraSphere 360 Y-90 Management PlatformLLZ · Special | Boston Scientific Corporation | 07/24/2026SE |
| K262143 | ImageGrid StreamVueLLZ · Traditional | Candelis, Inc. | 07/23/2026SE |
| K260500 | ResolutionMDLLZ · Traditional | ResolutionMD, Inc. | 07/21/2026SE |
| K262120 | Avara ViewerLLZ · Traditional | Avara Software | 07/10/2026SE |
More from Avara Software
| 510(k) | Device | Decision |
|---|---|---|
| K961740 | Kodak Digital Science Medical Printer Interface UnitLLZ · Traditional | 11/14/1996SE |
| K961768 | Kodak Digital Science Film Digitizer L7501/L7506 (with Film Autofeeder)LMA · Traditional | 08/22/1996SE |
| K960981 | Kodak Digital Science(Kds) Medical Image and Information LibraryLMB · Traditional | 06/07/1996SE |
| K951948 | Kodak XLS 8600 (PS)LMC · Traditional | 09/13/1995SE |
| K951807 | Kodak Ektascan Triad Laser Printer System, Photon Laser PrinterLMC · Traditional | 09/13/1995SE |
Questions and answers
When was Kodak Digital Science Medical Modality Acquisition Unit cleared by the FDA?
Kodak Digital Science Medical Modality Acquisition Unit (K961739) received a 510(k) decision of Substantially Equivalent on November 14, 1996, 195 days after the submission was received.
What is the product code of K961739?
The FDA product code is LLZ – System, Image Processing, Radiological, a Class II (moderate risk) device regulated under 21 CFR 892.2050.