Dlp, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CLEARVIEW BLOWER/MISTER, OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006), RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH ELONGATED & TREADED CUFF & INTRODUCER STYLET
56
Total
56
Cleared
0
Denied
FDA 510(k) Regulatory Record - Dlp, Inc. General Hospital ✕
3 devices