Data / Medical devices / United States / The Quality Assurance Service Corp.
The Quality Assurance Service Corp.: FDA-registered device maker in Martinez, GA, United States, 1 510(k) clearance
The Quality Assurance Service Corp. is registered with the FDA (registration 1032263) in Martinez, GA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 17, 1981. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 1032263
- Address
- 310 Commerce DR., Martinez, GA, United States, 30907
- Owner or operator
- THE QUALITY ASSURANCE SERVICE CORP. (1032263)
- Roles
- Manufacturer
- First device listed
- January 28, 2008
- Registered through
- 2027
- Brand names listed
- Quality Contol Material for Immunoassay and GSMS, Screen Plus and Minus Controls
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Drug Mixture Control Materials | DIF | 1 | 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 |
|---|---|---|---|---|---|---|
| December 17, 1981 | K812950 | QAC CONTROL | DIF | Substantially Equivalent | The Quality Assurance Service Corp. | accessdata.fda.gov |
Compare with other makers
Updated December 17, 1981. 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.