Data / Medical devices / Australia / Asp Plastics Pty Ltd.
Asp Plastics Pty Ltd.: FDA-registered device maker in ST-MARYS New South Wales, Australia, 1 510(k) clearance
Asp Plastics Pty Ltd. is registered with the FDA (registration 3003756985) in ST-MARYS New South Wales, Australia. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 25, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003756985
- Address
- 17 Harris ST., ST-MARYS New South Wales, Australia, 2760
- Owner or operator
- ASP PLASTICS PTY LTD. (9045378)
- Roles
- Exporter to the US, Manufacturer, Repackager or relabeler
- First device listed
- June 1, 2004
- Registered through
- 2026
- Brand names listed
- ASP Plastics Pty Ltd
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Container, Sharps | MMK | 2 | Exporter to the US, Manufacturer, 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 25, 2006 | K060037 | FITPACK | MMK | Substantially Equivalent | Asp Plastics Pty , Ltd. | accessdata.fda.gov |
Compare with other makers
Updated July 25, 2006. 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.