FDA 510(k) Applications Submitted by DLP, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K973485 | 09/15/1997 | CLEARVIEW BLOWER/MISTER | DLP, INC. |
| K964445 | 11/06/1996 | OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006) | DLP, INC. |
| K953945 | 08/21/1995 | RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH ELONGATED & TREADED CUFF & INTRODUCER STYLET | DLP, INC. |
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