Data / Medical devices / United States / Somavac Medical Solutions, Inc.
Somavac Medical Solutions, Inc.: FDA-registered device maker in Memphis, TN, United States, 1 510(k) clearance
Somavac Medical Solutions, Inc. is registered with the FDA (registration 3014827316) in Memphis, TN, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 31, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014827316
- Address
- 3144 Stage Post Drive Suite 101, Memphis, TN, United States, 38133
- Owner or operator
- Somavac Medical Solutions, Inc. (10058586)
- Roles
- Manufacturer
- First device listed
- October 11, 2018
- Registered through
- 2026
- Brand names listed
- Drain Connector, Lab Kit, Somavac 100
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Catheter | KGZ | 1 | Manufacturer | accessdata.fda.gov |
| Apparatus, Suction, Single Patient Use, Portable, Nonpowered | GCY | 1 | Manufacturer | accessdata.fda.gov |
| Container, Specimen Mailer And Storage, Sterile | KDT | 1 | Manufacturer | accessdata.fda.gov |
| Pump, Portable, Aspiration (Manual Or Powered) | BTA | 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 |
|---|---|---|---|---|---|---|
| May 31, 2018 | K180606 | SOMAVAC Device | BTA | Substantially Equivalent | Somavac Medical Solutions, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Accessories, Catheter
- All makers of Apparatus, Suction, Single Patient Use, Portable, Nonpowered
- All makers of Pump, Portable, Aspiration (Manual Or Powered)
- All makers of Container, Specimen Mailer And Storage, Sterile
Updated May 31, 2018. 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.