Data / Medical devices / Italy / Restech SRL
Restech SRL: FDA-registered device maker in Milano, Italy, 1 510(k) clearance
Restech SRL is registered with the FDA (registration 3012624216) in Milano, Italy. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 24, 2016. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012624216
- Address
- Via Melchiorre Gioia 61-63, Milano, Italy, 20124
- Owner or operator
- Restech Srl (10052425)
- Roles
- Manufacturer
- First device listed
- July 27, 2016
- Registered through
- 2026
- Brand names listed
- Resmon PRO FULL
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Impedance Measuring Device Utilizing Oscillation Techniques | PNV | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| June 24, 2016 | K152585 | Resmon PRO FULL | PNV | Substantially Equivalent | Medical Graphics Corp. | accessdata.fda.gov |
Compare with other makers
Updated June 24, 2016. 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.