FDA 510(k) Applications Submitted by RD CHUS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K971146 | 03/28/1997 | LAPARETTE | RD CHUS, INC. |
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FDA 510(k) Applications Submitted by RD CHUS, INC.
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