Parker Laboratories, Inc. - FDA 510(k) Cleared Devices
30
Total
30
Cleared
0
Denied
Parker Laboratories, Inc. has 30 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Latest FDA clearance: Aug 2024. Active since 1977. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Parker Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Parker Laboratories, Inc.
30 devices
Cleared
Aug 15, 2024
UltraDrape UGPIV Barrier and Securement (34-15)
Radiology
244d
Cleared
Mar 14, 1996
ECLIPSE PROBE COVER
Radiology
220d
Cleared
Feb 23, 1995
ULTRA COVER ULTRASOUND TRANSDUCER PROBE COVERS
Radiology
1051d
Cleared
Dec 01, 1986
AQUALUBE(TM)
General Hospital
12d
Cleared
Apr 17, 1986
ACRYLIC SOLDER
Dental
15d
Cleared
Mar 04, 1986
DYNA SYSTEM
Dental
68d
Cleared
Sep 27, 1985
POLYGEL ULTRASOUND GEL
Radiology
150d
Cleared
Aug 09, 1985
CONTACT CONDUCTIVE ADHESIVE GEL COMPOSITION
Neurology
29d
Cleared
Jun 15, 1984
NEURO PULSE
Neurology
73d
Cleared
Apr 17, 1984
RESIL
Dental
69d
Cleared
May 27, 1983
COMPLUS VARIOUS FORMS
Dental
57d
Cleared
Nov 03, 1982
ANTI-MIST, ANTI-FOG EYEGLASS & DENTAL
Gastroenterology & Urology
57d