Dlp, Inc. - FDA 510(k) Cleared Devices
56
Total
56
Cleared
0
Denied
FDA 510(k) Regulatory Record - Dlp, Inc. General & Plastic Surgery ✕
12 devices
Cleared
Apr 25, 1995
MACRO SUCTION TUBE MODEL NO 10061
General & Plastic Surgery
67d
Cleared
Jan 09, 1992
BREAST LES LOCAL WIRE ST. 48219/49220/48119/48120
General & Plastic Surgery
84d
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
Jan 03, 1990
MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI.
General & Plastic Surgery
79d
Cleared
Apr 18, 1989
CORE BIOPSY NEEDLE, CATALOG CODE #54006
General & Plastic Surgery
32d
Cleared
Feb 05, 1986
TOURIQUET KIT WITH SNARE
General & Plastic Surgery
41d
Cleared
Jun 04, 1985
ELECTRO-CAUTERY KNIFE CLEANER 6000 1
General & Plastic Surgery
15d
Cleared
Apr 24, 1984
INTRADISCAL THERAPY NEEDLE 18 GAUGE
General & Plastic Surgery
53d
Cleared
Mar 11, 1982
CATHETER, MULTIPLE LUMEN
General & Plastic Surgery
21d
Cleared
Jan 05, 1982
CUATICO MYELOGRAPHY NEEDLES
General & Plastic Surgery
36d
Cleared
Jan 05, 1982
DISPOSABLE CHIBA-TYPE NEEDLE
General & Plastic Surgery
36d