Data / Medical devices / Canada / C.M.P. Canadian Medical Products Inc.
C.M.P. Canadian Medical Products Inc.: FDA-registered device maker in Aurora Ontario, Canada, 7 510(k) clearances
C.M.P. Canadian Medical Products Inc. is registered with the FDA (registration 8022189) in Aurora Ontario, Canada. It lists 5 device types. The FDA files 7 510(k) clearances under its listings, the newest dated August 18, 2009. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 8022189
- FEI number
- 3004668996
- Address
- 7-10 Furbacher Lane, Aurora Ontario, Canada, L4G 6W1
- Owner or operator
- CMP CANADIAN MEDICAL PRODUCTS INC. (8022189)
- Roles
- Exporter to the US, Manufacturer, Repackager or relabeler
- First device listed
- May 20, 1999
- Registered through
- 2026
- Brand names listed
- CMP CABLES, CMP Neuropulse Combo, CMP Vacuum Leadwires, Mono Solution, Mono-DIN Adaptor, PROCARBON IFC ELECTRODES, PROFLEX ELECTRODES, Pals Platinum Neurostimulation Electrodes and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cable, Electrode | IKD | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Electrode, Cutaneous | GXY | 2 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Interferential Current Therapy | LIH | 2 | Repackager or relabeler | accessdata.fda.gov |
| Stimulator, Muscle, Powered | IPF | 2 | Repackager or relabeler | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | 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 |
|---|---|---|---|---|---|---|
| August 18, 2009 | K083250 | NEUROMED ELECTROANALGESIC DELIVERY SYSTEMS | GZJ | Substantially Equivalent | Aa Neuromed Corp. | accessdata.fda.gov |
| July 30, 2009 | K091236 | MANTRA COMBO, MODEL MECS 320 | GZJ | Substantially Equivalent | Mantra Intl. (Hk) , Ltd. | accessdata.fda.gov |
| February 2, 2001 | K002227 | WANDY SILICONE CONDUCTIVE RUBBER PAD | GXY | Substantially Equivalent | Wandy Rubber Industrial Co., Ltd. | accessdata.fda.gov |
| September 17, 1999 | K983097 | TENS/FES/NMES ELECTRODES | GXY | Substantially Equivalent | Uni-Patch, Inc. | accessdata.fda.gov |
| December 22, 1995 | K946230 | ENDURA REUSABLE TENS AND NMES ELECTRODES | GZJ | Substantially Equivalent | Selectivemed Components, Inc. | accessdata.fda.gov |
| June 18, 1985 | K852267 | ELECTRICAL NERVE STIMULATION(TENS) ELECTRODES | GXY | Substantially Equivalent | Axelgaard Mfg. Co., Ltd. | accessdata.fda.gov |
| May 10, 1984 | K841579 | MULTIPLEX I, INTERFERENTIAL CURRENT | IPF | Substantially Equivalent | Houwers Enterprises , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Electrode, Cutaneous
- All makers of Interferential Current Therapy
- All makers of Stimulator, Muscle, Powered
- All makers of Stimulator, Nerve, Transcutaneous, For Pain Relief
- All makers of Cable, Electrode
Updated August 18, 2009. 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.