Data / Medical devices / Canada / Jac-Cell Medic

Jac-Cell Medic: FDA-registered device maker in Mont - Royal Quebec, Canada, 1 510(k) clearance

Jac-Cell Medic is registered with the FDA (registration 3003008746) in Mont - Royal Quebec, Canada. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 28, 2017. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number

3003008746

Address

5764 Pare Street TMR, Mont - Royal Quebec, Canada, H4P 2M2

Owner or operator

Jac-Cell Medic (10085893)

Roles

Manufacturer

First device listed

September 16, 2022

Registered through

2027

Brand names listed

Jac-Cell Medic testers

Devices it lists

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.

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Updated February 28, 2017. 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.