Data / Medical devices / United Kingdom / Mardav Solutions Ltd
Mardav Solutions Ltd: FDA-registered device maker in Manchester, United Kingdom, 1 510(k) clearance
Mardav Solutions Ltd is registered with the FDA (registration 3016436764) in Manchester, United Kingdom. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 21, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016436764
- Address
- 205a Heywood Road, Manchester, United Kingdom, M25 0FU
- Owner or operator
- Mardav Solutions Ltd (10052345)
- Roles
- Exporter to the US
- First device listed
- March 3, 2024
- Registered through
- 2026
- Brand names listed
- Olympus, Philips
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Photographic, For Endoscope (Exclude Light Sources) | FEM | 1 | Exporter to the US | accessdata.fda.gov |
| Light Source, Endoscope, Xenon Arc | GCT | 2 | Exporter to the US | accessdata.fda.gov |
| System, Imaging, Pulsed Doppler, Ultrasonic | IYN | 2 | Exporter to the US | accessdata.fda.gov |
| System, Imaging, Pulsed Echo, Ultrasonic | IYO | 2 | Exporter to the US | accessdata.fda.gov |
| Transducer, Ultrasonic, Diagnostic | ITX | 2 | Exporter to the US | accessdata.fda.gov |
| Transformer, Endoscope | GCW | 2 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 21, 2013 | K132304 | EPIQ DIAGNOSTIC ULTRASOUND SYSTEM | IYN | Substantially Equivalent | Philips Ultrasound, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Light Source, Endoscope, Xenon Arc
- All makers of System, Imaging, Pulsed Echo, Ultrasonic
- All makers of System, Imaging, Pulsed Doppler, Ultrasonic
- All makers of Transducer, Ultrasonic, Diagnostic
- All makers of Accessories, Photographic, For Endoscope (Exclude Light Sources)
- All makers of Transformer, Endoscope
Updated August 21, 2013. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.