Data / Medical devices / Australia / Livac Pty Ltd
Livac Pty Ltd: FDA-registered device maker in Hawthorn Victoria, Australia, 1 510(k) clearance
Livac Pty Ltd is registered with the FDA (registration 3014273609) in Hawthorn Victoria, Australia. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 20, 2016. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014273609
- Address
- R1, 17 Lynch Street, Hawthorn Victoria, Australia, 3122
- Owner or operator
- Livac Pty Ltd (10060369)
- Roles
- Specification developer
- First device listed
- July 11, 2019
- Registered through
- 2026
- Brand names listed
- Livac Retractor System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Laparoscope, General & Plastic Surgery | GCJ | 2 | 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 |
|---|---|---|---|---|---|---|
| October 20, 2016 | K162445 | LiVac Retractor System | GCJ | Substantially Equivalent | Livac Pty, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated October 20, 2016. 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.