Data / Medical devices / Canada / Datrend Systems Inc
Datrend Systems Inc: FDA-registered device maker in RICHMOND British Columbia, Canada, 1 510(k) clearance
Datrend Systems Inc is registered with the FDA (registration 9615335) in RICHMOND British Columbia, Canada. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 25, 2007. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9615335
- FEI number
- 3002806858
- Address
- 4020 Viking Way Unit 130, RICHMOND British Columbia, Canada, V6V 2L4
- Owner or operator
- Datrend Systems Inc (9032342)
- Roles
- Manufacturer
- First device listed
- November 4, 2008
- Registered through
- 2026
- Brand names listed
- Phase3 Defibrillator/Pacer Analyzer
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Tester, Defibrillator | DRL | 2 | 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 25, 2007 | K062099 | PHASE 3, MODEL DT-1 | DRL | Substantially Equivalent | Datrend Systems, Inc. | accessdata.fda.gov |
Compare with other makers
Updated January 25, 2007. 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.