Data / Medical devices / United States / Tucker Designs, Ltd.
Tucker Designs, Ltd.: FDA-registered device maker in Metairie, LA, United States, 1 510(k) clearance
Tucker Designs, Ltd. is registered with the FDA (registration 2319127) in Metairie, LA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 26, 1994. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2319127
- FEI number
- 1000112533
- Address
- 701 Papworth Ave Ste 101, Metairie, LA, United States, 70005
- Owner or operator
- TUCKER DESIGNS, LTD. (9004539)
- Roles
- Manufacturer
- First device listed
- December 7, 2007
- Registered through
- 2026
- Brand names listed
- Tucker Sling
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Holder, Infant Position | FRP | 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 |
|---|---|---|---|---|---|---|
| January 26, 1994 | K932636 | THE TUCKER SLING | FRP | Substantially Equivalent | Tucker Designs, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated January 26, 1994. 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.