Data / Medical devices / United States / AmeriPac, inc. - 951 Mustang Dr
AmeriPac, inc. - 951 Mustang Dr: FDA-registered device maker in Grapevine, TX, United States, 1 510(k) clearance
AmeriPac, inc. - 951 Mustang Dr is registered with the FDA (registration 3018326554) in Grapevine, TX, United States. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 9, 2009. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3018326554
- Address
- 951 Mustang Dr, Grapevine, TX, United States, 76051
- Owner or operator
- Veritiv Operating Company (10092683)
- Roles
- Repackager or relabeler
- First device listed
- February 5, 2025
- Registered through
- 2026
- Brand names listed
- Disposable hot or cold pack, Easy Touch Insulin Syringe, Emesis basin, HealX, Sanitary Pads
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Basin, Emesis | FNY | 1 | Repackager or relabeler | accessdata.fda.gov |
| Pack, Hot Or Cold, Disposable | IMD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Pad, Menstrual, Unscented | HHD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Repackager or relabeler | accessdata.fda.gov |
| Tape, Measuring, Rulers And Calipers | FTY | 1 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| July 9, 2009 | K091474 | EASY.TOUCH INSULIN SYRINGE | FMF | Substantially Equivalent | Masters Healthcare, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Tape, Measuring, Rulers And Calipers
- All makers of Pack, Hot Or Cold, Disposable
- All makers of Basin, Emesis
- All makers of Pad, Menstrual, Unscented
- All makers of Syringe, Piston
Updated July 9, 2009. 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.