Hogan & Hartson is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hogan & Hartson - FDA 510(k) Cleared Devices
26
Total
25
Cleared
0
Denied
Hogan & Hartson has 25 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 25 cleared submissions from 1980 to 1998.
Browse the FDA 510(k) cleared devices submitted by Hogan & Hartson Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hogan & Hartson
26 devices
Cleared
Jan 23, 1998
COOPERSURGICAL INFRARED COAGULATOR
Gastroenterology & Urology
79d
Cleared
Jan 06, 1998
BIOABSORBABLE BANKART TACK
Orthopedic
90d
Cleared
Nov 20, 1997
DUAL RADIATION TARGETING SYSTEM DRTS DRAPE
General Hospital
90d
Cleared
May 23, 1996
RIBOSOMAL P EIA TEST SYSTEM
Immunology
492d
Cleared
Feb 16, 1996
TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES
Obstetrics & Gynecology
639d
Cleared
Jan 24, 1996
CARDIOLIPIN G EIA TEST SYSTEM
Immunology
399d
Cleared
Jan 24, 1996
CARDIOLIPIN A EIA TEST SYSTEM
Immunology
399d
Cleared
Jan 24, 1996
CARDIOLIPIN M EIA TEST SYSTEM
Immunology
399d
Cleared
Aug 14, 1995
CHAL-2500
Physical Medicine
237d
Cleared
Jun 30, 1995
COMPUSPEAK
Radiology
455d
Cleared
May 15, 1995
MARDX ENA EIA TEST SYSTEM
Immunology
145d
Cleared
May 15, 1995
MARDX MITOCHONDRIA EIA TEST SYSTEM
Immunology
124d