FDA 510(k) Applications Submitted by BEACON ENDOSCOPIC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K133008 | 09/25/2013 | BNX DELIVERY SYSTEM PRE-LOADED WITH 19, 22 AND 25 GAUGE NEEDLE, 19, 22 OR 25 GAUGE NEEDLES (INDIVIDUALLY STERILE-PACKED, | BEACON ENDOSCOPIC |
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