Data / Medical devices / United States / Integrated Biomedical Corp.
Integrated Biomedical Corp.: FDA-registered device maker in Las Vegas, NV, United States, 5 510(k) clearances
Integrated Biomedical Corp. is registered with the FDA (registration 3004413879) in Las Vegas, NV, United States. It lists 3 device types. The FDA files 5 510(k) clearances under its listings, the newest dated February 2, 1990. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004413879
- Address
- 4481 W. Reno Ave, Las Vegas, NV, United States, 89118
- Owner or operator
- INTEGRATED BIOMEDICAL CORP. (9060302)
- Roles
- Manufacturer
- First device listed
- December 10, 2007
- Registered through
- 2026
- Brand names listed
- ALGONIX, Electro-Acuscope 70C, Electro-Acuscope 80, Electro-Acuscope 80C, Electro-Acuscope 80L, Electro-Acuscope 85, Electro-Acuscope 85P, Electro-Equiscope and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electromyograph, Diagnostic | IKN | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Muscle, Powered | IPF | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| February 2, 1990 | K883911 | ELECTRO-ACUSCOPE 85 | GZJ | Substantially Equivalent | Biomedical Design Instruments | accessdata.fda.gov |
| December 14, 1984 | K833928 | MYOPULSE | IPF | Substantially Equivalent | Biomedical Design Instruments | accessdata.fda.gov |
| December 27, 1983 | K833927 | ELECTRO-MYOSCOPE 85 | IKN | Substantially Equivalent | Biomedical Design Instruments | accessdata.fda.gov |
| October 31, 1983 | K832442 | ELECTRO-ACUSCOPE | GZJ | Substantially Equivalent | Kenneth J. Purcell | accessdata.fda.gov |
| August 20, 1980 | K801459 | ELECTRO-ACUSCOPE-70 | GZJ | Substantially Equivalent | Nebrensky Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Stimulator, Nerve, Transcutaneous, For Pain Relief
- All makers of Stimulator, Muscle, Powered
- All makers of Electromyograph, Diagnostic
Updated February 2, 1990. 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.