FDA 510(k) Applications Submitted by SKD, INC. A BECKMAN COULTER CO.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K981512 | 04/28/1998 | ICON FXHCG URINE/SERUM TEST, ICON FXHCG URINE TEST, MODELS 40025,40050, 40005 & 41025 | SKD, INC. A BECKMAN COULTER CO. |
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