FDA 510(k) Applications Submitted by Okapi Medical LLC dba Resivant Medical
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K234114 | 12/27/2023 | CUTIVA(TM) Topical Skin Adhesive (RM-1700); CUTIVA(TM) PLUS Skin Closure System (RM-1739) | Okapi Medical LLC dba Resivant Medical |
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