Data / Medical devices / United States / Tasso Inc
Tasso Inc: FDA-registered device maker in Seattle, WA, United States, 1 510(k) clearance
Tasso Inc is registered with the FDA (registration 3012172036) in Seattle, WA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 12, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012172036
- Address
- 400 2nd Ave W, Seattle, WA, United States, 98119
- Owner or operator
- Tasso Inc (10061412)
- Roles
- Complaint file establishment, Manufacturer, Manufacturer for export
- First device listed
- October 15, 2019
- Registered through
- 2026
- Brand names listed
- Tasso 3, Tasso Mini, Tasso Mini Standard Kit, Tasso+, Tasso+ Standard Kit, Tasso-M20, Tile-T20
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Blood Specimen Collection Convenience Kit (Excludes Hiv) | PQD | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Container, Specimen Mailer And Storage, Non-Sterile | NNK | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature | FMK | 2 | Complaint file establishment, Manufacturer, Manufacturer for export | 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 12, 2022 | K221131 | Tasso+ | FMK | Substantially Equivalent | Tasso, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Blood Specimen Collection Convenience Kit (Excludes Hiv)
- All makers of Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
- All makers of Container, Specimen Mailer And Storage, Non-Sterile
Updated August 12, 2022. 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.