Horizons Intl. Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Horizons Intl. Corp. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Horizons Intl. Corp. has 10 FDA 510(k) cleared gastroenterology & urology devices. Based in Aguadilla, US.
Historical record: 10 cleared submissions from 2001 to 2008.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Horizons Intl. Corp.
10 devices
Cleared
Dec 23, 2008
TORNADO ROTATABEL SNARE AND POLYP CATCHER
Gastroenterology & Urology
70d
Cleared
Oct 25, 2002
HORIZONS REUSABLE HOT BIOPSY FORCEPS
Gastroenterology & Urology
105d
Cleared
Oct 25, 2002
HORIZONS REUSABLE POLYPECTOMY SNARES
Gastroenterology & Urology
102d
Cleared
Aug 12, 2002
HORIZONS ANSO TRANSBRONCHIAL ASPIRATION NEEDLES
Ear, Nose, Throat
11d
Cleared
Jul 12, 2002
HORIZONS CYTOLOGY BRUSH
Gastroenterology & Urology
23d
Cleared
Jun 21, 2002
HORIZONS HOT BIOPSY FORCEPS
Gastroenterology & Urology
29d
Cleared
Aug 16, 2001
HORIZONS INTERNATIONAL POLYPECTOMY SNARES
Gastroenterology & Urology
78d
Cleared
May 16, 2001
HORIZONS INTERNATIONAL VARICES INJECTION NEEDLES
Gastroenterology & Urology
90d
Cleared
Jan 23, 2001
HORIZONS ERCP CANNULA
Gastroenterology & Urology
183d
Cleared
Jan 23, 2001
HORIZONS PAPILLOTOME
Gastroenterology & Urology
183d