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GB ACT + KIT
 Request for Information Form |
 Contact Information
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| Company Name | SIENCO, INC. |
| Address | 7985 N. VANCE DR., SUITE 104 |
| City, State, Zip | ARVADA, CO 80003 |
| Country | US |
| FDA Owner/Operator Phone | 303-420-1148 |
| FDA Medical Specialty Code | HE - Hematology |
| FDA Product Code | JBP |
| FDA Classification Name | ACTIVATED WHOLE BLOOD CLOTTING TIME |
| FDA Device Classification Code | Standards |
| FDA Regulation Number | 864.7140 |
| FDA Common Generic Name | ACT TEST |
| FDA Proprietary Device Name | GB ACT + KIT |
| FDA Owner / Operator Number | 1719400 |
| FDA Owner / Operator Name | SIENCO, INC. |
| FDA Establishment Registration Number | 1719400 |
| FDA Registered Establishment Name | SIENCO, INC. |
| FDA Operation Code(s) |
MM - Manufacturer |
| FDA Listing Date | 10-17-00 |
| FDA Listing Status Code | Active |
| Differentiation | N/A |
| Keywords | N/A |
| Description | N/A |
| Brochure | N/A |
| Product Website | N/A |
Competitors of SIENCO, INC.
Our records indicate that the following medical device companies may manufacture a similar device.
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