Data / Medical devices / United States / AG Industries LLC
AG Industries LLC: FDA-registered device maker in Fairburn, GA, United States, 1 510(k) clearance
AG Industries LLC is registered with the FDA (registration 3004874794) in Fairburn, GA, United States. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 4, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004874794
- Address
- 500 Bohannon Rd, Fairburn, GA, United States, 30213
- Owner or operator
- AG Industries (9041666)
- Roles
- Manufacturer
- First device listed
- August 30, 2010
- Registered through
- 2026
- Brand names listed
- AG APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED, AG BOTTLE, COLLECTION, VACUUM, AG CANNULA, NASAL, OXYGEN, AG Filter, bacterial, breathing-circuit, AG TUBING, NONINVASIVE, AG TUBING, PRESSURE AND ACCESSORIES
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Suction, Operating-Room, Wall Vacuum Powered | GCX | 2 | Manufacturer | accessdata.fda.gov |
| Bottle, Collection, Vacuum | KDQ | 2 | Manufacturer | accessdata.fda.gov |
| Cannula, Nasal, Oxygen | CAT | 1 | Manufacturer | accessdata.fda.gov |
| Filter, Bacterial, Breathing-Circuit | CAH | 2 | Manufacturer | accessdata.fda.gov |
| Tubing, Noninvasive | GAZ | 2 | Manufacturer | accessdata.fda.gov |
| Tubing, Pressure And Accessories | BYX | 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 |
|---|---|---|---|---|---|---|
| February 4, 2010 | K091363 | COMPRESSOR FILTER, MODELS AG1038831, HCF100,BF900,BF910,BF950, LL201, LL202, LL205, BACTERIA FILTER | CAH | Substantially Equivalent | Ag Industries | accessdata.fda.gov |
Compare with other makers
- All makers of Apparatus, Suction, Operating-Room, Wall Vacuum Powered
- All makers of Filter, Bacterial, Breathing-Circuit
- All makers of Bottle, Collection, Vacuum
- All makers of Tubing, Noninvasive
- All makers of Cannula, Nasal, Oxygen
- All makers of Tubing, Pressure And Accessories
Updated February 4, 2010. 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.