Data / Medical devices / United States / Mada Medical Products, Inc.
Mada Medical Products, Inc.: FDA-registered device maker in Carlstadt, NJ, United States, 2 510(k) clearances
Mada Medical Products, Inc. is registered with the FDA (registration 2225311) in Carlstadt, NJ, United States. It lists 11 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 16, 2004. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2225311
- Address
- 625 Washington Ave., Carlstadt, NJ, United States, 07072
- Owner or operator
- MADA MEDICAL PRODUCTS, INC. (2225311)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- October 6, 1992
- Registered through
- 2026
- Brand names listed
- BACK-PRESSURE COMPENSATED, FLOWMETER, MadaCide-FD, MadaCide-1, MadaCide-FDW-Plus, MadaVac, Madajet, THROPE, TUBE
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Suction, Ward Use, Portable, Ac-Powered | JCX | 2 | Repackager or relabeler | accessdata.fda.gov |
| Cannula, Nasal, Oxygen | CAT | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Cart, Emergency, Cardiopulmonary (Excluding Equipment) | BZN | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Disinfectant, Medical Devices | LRJ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Disinfector, Medical Devices | MEC | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Flowmeter, Tube, Thorpe, Back-Pressure Compensated | CAX | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Injector, Fluid, Non-Electrically Powered | KZE | 2 | Manufacturer | accessdata.fda.gov |
| Injector, Jet, Mechanical-Powered | EGM | 2 | Manufacturer | accessdata.fda.gov |
| Mask, Oxygen | BYG | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Pump, Nebulizer, Manual | EPN | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Regulator, Pressure, Gas Cylinder | CAN | 1 | Manufacturer, 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 |
|---|---|---|---|---|---|---|
| December 16, 2004 | K042349 | EMG MODEL SUA01 SUCTION UNIT | JCX | Substantially Equivalent | Emg Technology Co., Ltd. | accessdata.fda.gov |
| December 10, 1985 | K850754 | MEDAJET XL - JET INJECTOR | KZE | Substantially Equivalent | Mada Medical Products, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Cart, Emergency, Cardiopulmonary (Excluding Equipment)
- All makers of Pump, Nebulizer, Manual
- All makers of Mask, Oxygen
- All makers of Disinfector, Medical Devices
- All makers of Disinfectant, Medical Devices
- All makers of Flowmeter, Tube, Thorpe, Back-Pressure Compensated
Updated December 16, 2004. 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.