Data / Medical devices / Sweden / AB Mando
AB Mando: FDA-registered device maker in HUDDINGE Stockholm, Sweden, 1 510(k) clearance
AB Mando is registered with the FDA (registration 3009128345) in HUDDINGE Stockholm, Sweden. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 31, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009128345
- Address
- Halsovagen 7, HUDDINGE Stockholm, Sweden, S-141 04
- Owner or operator
- AB Mando (10036109)
- Roles
- Manufacturer
- First device listed
- April 20, 2011
- Registered through
- 2026
- Brand names listed
- Mandometer
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Eating Disorder Conditioning Tool | OBV | 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 |
|---|---|---|---|---|---|---|
| March 31, 2011 | DEN070014 | MANDOMETER III | OBV | Unknown | Ab Mando | accessdata.fda.gov |
Updated March 31, 2011. 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.