Data / Medical devices / United States / W.T. Farley, Inc.
W.T. Farley, Inc.: FDA-registered device maker in Ladson, SC, United States, 1 510(k) clearance
W.T. Farley, Inc. is registered with the FDA (registration 2080309) in Ladson, SC, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 12, 1978. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 2080309
- Address
- 9551 Palmetto Commerce Parkway BLDG 100, Ladson, SC, United States, 29456
- Owner or operator
- W.T. FARLEY, INC. (2080309)
- Roles
- Manufacturer, Specification developer
- First device listed
- June 23, 2008
- Registered through
- 2027
- Brand names listed
- Accessories Only, CS-ARM, CS-ARM-2, CS-ARM-3, DU-O-VAC
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Suction, Operating-Room, Wall Vacuum Powered | GCX | 2 | Manufacturer | accessdata.fda.gov |
| Bed, Ac-Powered Adjustable Hospital | FNL | 2 | Manufacturer | accessdata.fda.gov |
| Support, Breathing Tube | JAY | 1 | Specification developer | 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 12, 1978 | K781988 | SUCTION APPARATUS, POWERED BY COMP. AIR | GCX | Substantially Equivalent | Farley, W.T. | accessdata.fda.gov |
Compare with other makers
- All makers of Bed, Ac-Powered Adjustable Hospital
- All makers of Apparatus, Suction, Operating-Room, Wall Vacuum Powered
- All makers of Support, Breathing Tube
Updated December 12, 1978. 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.