Data / Medical devices / Canada / Chg-Meridian Canada Ltd
Chg-Meridian Canada Ltd: FDA-registered device maker in Mississauga Ontario, Canada, 5 510(k) clearances
Chg-Meridian Canada Ltd is registered with the FDA (registration 3023102955) in Mississauga Ontario, Canada. It lists 10 device types. The FDA files 5 510(k) clearances under its listings, the newest dated January 10, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3023102955
- Address
- 1 Robert Speck Parkway, Suite No. 960, Mississauga Ontario, Canada, L4Z 3M3
- Owner or operator
- CHG-MERIDIAN CANADA LTD (10085392)
- Roles
- Exporter to the US
- First device listed
- June 14, 2022
- Registered through
- 2026
- Brand names listed
- Scope Broncho Video, Scope Colono Video Scope, Scope Cysto Battery Fiberoptic, Scope Cysto Videoscope, Scope Rhino Fiberoptic
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bronchoscope (Flexible Or Rigid) | EOQ | 2 | Exporter to the US | accessdata.fda.gov |
| Colonoscope And Accessories, Flexible/Rigid | FDF | 2 | Exporter to the US | accessdata.fda.gov |
| Cystoscope And Accessories, Flexible/Rigid | FAJ | 2 | Exporter to the US | accessdata.fda.gov |
| Endoscope, Accessories, Narrow Band Spectrum | NWB | 2 | Exporter to the US | accessdata.fda.gov |
| Forceps, Biopsy, Electric | KGE | 2 | Exporter to the US | accessdata.fda.gov |
| Forceps, Biopsy, Non-Electric | FCL | 1 | Exporter to the US | accessdata.fda.gov |
| Kit, Nephroscope | FGA | 2 | Exporter to the US | accessdata.fda.gov |
| Nasopharyngoscope (Flexible Or Rigid) | EOB | 2 | Exporter to the US | accessdata.fda.gov |
| Snare, Flexible | FDI | 2 | Exporter to the US | accessdata.fda.gov |
| Unit, Electrosurgical, Endoscopic (With Or Without Accessories) | KNS | 2 | Exporter to the US | 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 10, 2013 | K121959 | EVIS EXERA III VIDEO SYSTEM | EOQ | Substantially Equivalent | Olympus Medical Systems Corp. | accessdata.fda.gov |
| February 16, 2012 | K112680 | EVIS EXERA III VIDEO SYSTEM | FDF | Substantially Equivalent | Olympus Medical Systems Corporation | accessdata.fda.gov |
| September 22, 2006 | K062049 | EVIS EXERA II 180 SYSTEM | NWB | Substantially Equivalent | Olympus Medical Systems Corporation | accessdata.fda.gov |
| July 16, 2003 | K032092 | OLYMPUS XCYF-TP3 CYSTOFIBERSCOPE/NEPHROFIBERSCOPE | FCL | Substantially Equivalent | Olympus Optical Co., Ltd. | accessdata.fda.gov |
| July 25, 2001 | K011869 | XENF-DP RHINO-LARYNGOFIBERSCOPE, ITS ACCESSORIES AND ANCILLARY EQUIPMENT | EOB | Substantially Equivalent | The Olympus Optical Co. | accessdata.fda.gov |
Compare with other makers
- All makers of Bronchoscope (Flexible Or Rigid)
- All makers of Endoscope, Accessories, Narrow Band Spectrum
- All makers of Nasopharyngoscope (Flexible Or Rigid)
- All makers of Colonoscope And Accessories, Flexible/Rigid
- All makers of Snare, Flexible
- All makers of Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
Updated January 10, 2013. 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.