|
BIOCHECK IGE EIA TEST KIT
 Request for Information Form |
 Contact Information
|
| Company Name | BIOCHECK, INC. |
| Address | 323 VINTAGE PARK DR. |
| City, State, Zip | FOSTER CITY, CA 94404 |
| Country | US |
| FDA Owner/Operator Phone | -- |
| FDA Medical Specialty Code | IM - Immunology |
| FDA Product Code | JHR |
| FDA Classification Name | RADIOIMMUNOASSAY, IMMUNOGLOBULINS (D, E) |
| FDA Device Classification Code | Standards |
| FDA Regulation Number | 866.5510 |
| FDA Common Generic Name | IMMUNOGLOBULIN E EIA TEST KIT |
| FDA Proprietary Device Name | BIOCHECK IGE EIA TEST KIT |
| FDA Owner / Operator Number | 9033543 |
| FDA Owner / Operator Name | BIOCHECK, INC. |
| FDA Establishment Registration Number | 2953756 |
| FDA Registered Establishment Name | BIOCHECK, INC. |
| FDA Operation Code(s) |
MM - Manufacturer MR - Remanufacturer RR - Repackager/Relabeller |
| FDA Listing Date | 04-16-98 |
| FDA Listing Status Code | Active |
| Differentiation | N/A |
| Keywords | N/A |
| Description | N/A |
| Brochure | N/A |
| Product Website | N/A |
Competitors of BIOCHECK, INC.
Our records indicate that the following medical device companies may manufacture a similar device.
[ Lab Equipment Categories ]
Copyright © 2000-2009
All Rights Reserved - Patent Pending
