Bayer Corp. · Class I · Cleared May 2, 1995
| K-number | K951360 |
| Device name | ESTRADIOL ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM IN-VITRO DIAGNOSTIC SYSTEM |
| Applicant | Bayer Corp. |
| Product code | CHP |
| Device class | Class I |
| Decision date | May 2, 1995 |
| Decision | Substantially Equivalent |
| Regulation | 862.1260 |
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