FDA 510(k) Applications Submitted by DUNCAN HYND ASSOCIATES, LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K981911 | 06/01/1998 | PROFA | DUNCAN HYND ASSOCIATES, LTD. |
| K002608 | 08/21/2000 | INVAC | DUNCAN HYND ASSOCIATES, LTD. |
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