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MYOGLOBIN EIA KIT
 Request for Information Form |
 Contact Information
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| Company Name | BIOMERICA, INC. |
| Address | 1533 MONROVIA AVE. |
| City, State, Zip | NEWPORT BEACH, CA 92663 |
| Country | US |
| FDA Owner/Operator Phone | 949-645-2111 |
| FDA Medical Specialty Code | CV - Cardiovascular |
| FDA Product Code | DRR |
| FDA Classification Name | AMPLIFIER AND SIGNAL CONDITIONER, BIOPOTENTIAL |
| FDA Device Classification Code | Standards |
| FDA Regulation Number | 870.2050 |
| FDA Common Generic Name | MYOGLOBIN TEST KIT |
| FDA Proprietary Device Name | MYOGLOBIN EIA KIT |
| FDA Owner / Operator Number | 2016793 |
| FDA Owner / Operator Name | BIOMERICA, INC. |
| FDA Establishment Registration Number | 2016793 |
| FDA Registered Establishment Name | BIOMERICA, INC. |
| FDA Operation Code(s) |
RR - Repackager/Relabeller |
| FDA Listing Date | 09-20-06 |
| FDA Listing Status Code | Active |
| Differentiation | N/A |
| Keywords | N/A |
| Description | N/A |
| Brochure | N/A |
| Product Website | N/A |
Competitors of BIOMERICA, INC.
Our records indicate that the following medical device companies may manufacture a similar device.
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