Mammodiagnost DR
FDA 510(k) K110572 · Philips Medical Systems
510(k) numberK110572
Submission
- Device name
- Mammodiagnost DR
- Applicant
- Philips Medical Systems
Andover, MA, US - Received
- March 1, 2011
- Decision date
- September 23, 2011
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Other 510(k)s with product code MUE
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K254090 | I-View®MUE · Traditional | Hologic, Inc. | 09/02/2026SE |
| K253678 | MAMMOMAT B.brilliant (11372950)MUE · Traditional | Siemens Medical Solutions USA, Inc. | 06/18/2026SE |
| K254092 | Bellalun 2D (VDMS-1000S)MUE · Traditional | Vieworks Co., Ltd. | 05/28/2026SE |
| K260087 | Senographe Pristina; SenoBright HD; Pristina Serena; Pristina Serena BrightMUE · Traditional | GE Medical Systems SCS | 03/24/2026SE |
| K243420 | HestiaMUE · Traditional | Genoray Co., Ltd. | 07/17/2025SE |
| K243849 | 2430TCA with Xmaru WMUE · Special | Rayence Co., Ltd. | 03/12/2025SE |
| K241113 | Vivix-MMUE · Traditional | Vieworks Co., Ltd. | 01/16/2025SE |
| K233539 | MAMMOMAT B.brilliantMUE · Traditional | Siemens Medical Solutions USA, Inc. | 03/27/2024SE |
| K220073 | RMF-2000MUE · Traditional | DRTECH Corporation | 01/26/2023SE |
| K211720 | Planmed Clarity 2D, Planmed Clarify SMUE · Traditional | Planmed OY | 07/18/2022SE |
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| K191738 | PageWriter TC20 Cardiograph, PageWriter TC30 Cardiograph, PageWriter TC50 Cardiograph…DPS · Traditional | 09/29/2020SE |
| K192875 | Philips Biosensor BX100DRG · Traditional | 04/16/2020SE |
| K183387 | M3290B Patient Information Center iXMHX · Traditional | 08/06/2019SE |
| K180017 | MX40 Release C.01MHX · Special | 07/24/2018SE |
| K172226 | MX40 Release B.07MHX · Traditional | 11/09/2017SE |
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Questions and answers
When was Mammodiagnost DR cleared by the FDA?
Mammodiagnost DR (K110572) received a 510(k) decision of Substantially Equivalent on September 23, 2011, 206 days after the submission was received.
What is the product code of K110572?
The FDA product code is MUE – Full Field Digital, System, X-Ray, Mammographic, a Class II (moderate risk) device regulated under 21 CFR 892.1715.