Dlp, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
56
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K973485CLEARVIEW BLOWER/MISTERDecember 8, 1997
K964445OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006)January 30, 1997
K953945RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH ELONGATED & TREADED CUFF & INTRODUCER STYLETMarch 26, 1996
K950754MACRO SUCTION TUBE MODEL NO 10061April 25, 1995
K934215CONTAIN-ORFebruary 9, 1994
K915268CATHETER TWO STAGE VENOUS RETURNJuly 27, 1992
K913077LANCASTER COOLING JACKET, CAT. CODE #13500/13501January 9, 1992
K914608BREAST LES LOCAL WIRE ST. 48219/49220/48119/48120January 9, 1992
K913098APIRATION BIOPSY SYRINGE GUN, CAT. CODE #54501November 5, 1991
K912229IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003September 25, 1991
K904172ACCUPLACE (TM)November 21, 1990
K900994ANTEGRADE/RETROGRADE Y W/INTEGRAL SELECTOR SWIT.August 15, 1990
K901074CODE #94315 RETROGRADE CORONARY SINUS PERF CANNULAJuly 6, 1990
K900082MAXX 470 CORE BIOPSY GUNJune 27, 1990
K897022PICSO CANNULA, CATALOG CODE 94315March 16, 1990
K896019MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI.January 3, 1990
K893418MYOCARDIAL PROBE THERMOMETER CODE 64000September 5, 1989
K891537CORE BIOPSY NEEDLE, CATALOG CODE #54006April 18, 1989
K890707PHRENIC NERVE PAD & NERVE PAD W/1/4 PERCARDIALApril 10, 1989
K890453REUSABLE MLYOCARDIAL BIOPSY FORCEPS (BIOPTOMESMarch 31, 1989