FDA 510(k) Applications Submitted by PEREGRINE SURGICAL, LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K132614 | 08/21/2013 | PEREGRINE CURVED ILLUMINATING LASER PROBE | PEREGRINE SURGICAL, LTD. |
| K122905 | 09/21/2012 | PEREGRINE 23GA CURVED LASER PROBE | PEREGRINE SURGICAL, LTD. |
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