FDA 510(k) Applications Submitted by JOHN HOLLOWAY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K972185 | 06/10/1997 | 20 ML NORMAL SALINE TOPICAL SOLUTION, 0.9% W/V SODIUM CHLORIDE | STERIPAK, LTD. |
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