Dlp, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dlp, Inc. - FDA 510(k) Cleared Devices
56
Total
56
Cleared
0
Denied
Dlp, Inc. has 56 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 56 cleared submissions from 1979 to 1997. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Dlp, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dlp, Inc.
56 devices
Cleared
Dec 08, 1997
CLEARVIEW BLOWER/MISTER
General Hospital
84d
Cleared
Jan 30, 1997
OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006)
Cardiovascular
85d
Cleared
Mar 26, 1996
RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH ELONGATED & TREADED CUFF &...
Cardiovascular
218d
Cleared
Apr 25, 1995
MACRO SUCTION TUBE MODEL NO 10061
General & Plastic Surgery
67d
Cleared
Feb 09, 1994
CONTAIN-OR
General Hospital
163d
Cleared
Jul 27, 1992
CATHETER TWO STAGE VENOUS RETURN
Cardiovascular
245d
Cleared
Jan 09, 1992
LANCASTER COOLING JACKET, CAT. CODE #13500/13501
Cardiovascular
182d
Cleared
Jan 09, 1992
BREAST LES LOCAL WIRE ST. 48219/49220/48119/48120
General & Plastic Surgery
84d
Cleared
Nov 05, 1991
APIRATION BIOPSY SYRINGE GUN, CAT. CODE #54501
Gastroenterology & Urology
116d
Cleared
Sep 25, 1991
IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003
General & Plastic Surgery
128d
Cleared
Nov 21, 1990
ACCUPLACE (TM)
General & Plastic Surgery
71d
Cleared
Aug 15, 1990
ANTEGRADE/RETROGRADE Y W/INTEGRAL SELECTOR SWIT.
Cardiovascular
166d
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