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ANDROSTENEDIONE ENZYME IMMUNOASSAY TEST SYSTEM (EIA)
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 Contact Information
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| Company Name | DIAGNOSTICS BIOCHEM CANADA, INC. |
| Address | 1020 HARGRIEVE RD. |
| City, State, Zip | LONDON, ONTARIO, |
| Country | CA |
| FDA Owner/Operator Phone | 519-681-8731 |
| FDA Medical Specialty Code | CH - Clinical Chemistry |
| FDA Product Code | CIZ |
| FDA Classification Name | RADIOIMMUNOASSAY, ANDROSTENEDIONE |
| FDA Device Classification Code | General Controls |
| FDA Regulation Number | 862.1075 |
| FDA Common Generic Name | ANDROSTENEDIONE ENZYME IMMUNOASSAY TEST SYSTEM |
| FDA Proprietary Device Name | ANDROSTENEDIONE ENZYME IMMUNOASSAY TEST SYSTEM (EIA) |
| FDA Owner / Operator Number | 8010132 |
| FDA Owner / Operator Name | DIAGNOSTICS BIOCHEM CANADA, INC. |
| FDA Establishment Registration Number | 8010132 |
| FDA Registered Establishment Name | DIAGNOSTICS BIOCHEM CANADA, INC. |
| FDA Operation Code(s) |
MM - Manufacturer |
| FDA Listing Date | 12-07-01 |
| FDA Listing Status Code | Active |
| Differentiation | N/A |
| Keywords | N/A |
| Description | N/A |
| Brochure | N/A |
| Product Website | N/A |
Competitors of DIAGNOSTICS BIOCHEM CANADA, INC.
Our records indicate that the following medical device companies may manufacture a similar device.
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