FDA 510(k) Applications Submitted by HENNIG ENTERPRISES EUROPE S.R.L.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K020421 | 02/07/2002 | GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES | HENNIG ENTERPRISES EUROPE S.R.L. |
| K020424 | 02/08/2002 | V SET | HENNIG ENTERPRISES EUROPE S.R.L. |
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