Data / Medical devices / United States / Marc Pro, Inc.
Marc Pro, Inc.: FDA-registered device maker in Huntington Beach, CA, United States, 2 510(k) clearances
Marc Pro, Inc. is registered with the FDA (registration 3011050674) in Huntington Beach, CA, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated January 24, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011050674
- Address
- 5702 Bolsa Ave, Huntington Beach, CA, United States, 92649
- Owner or operator
- Marc Pro, Inc. (10047121)
- Roles
- Specification developer
- First device listed
- July 2, 2014
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Specification developer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 2 | Specification developer | 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 24, 2014 | K131910 | MPP | NUH | Substantially Equivalent | Marc Pro | accessdata.fda.gov |
| July 9, 2009 | K081998 | H-WAVE SPORT | NGX | Substantially Equivalent | Electronic Waveform Laboratory, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Stimulator, Muscle, Powered, For Muscle Conditioning
- All makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter
Updated January 24, 2014. 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.