ClearanceBrief
Company ยท US

Horizons Intl. Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2008. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FDISnare, Flexible3
KGEForceps, Biopsy, Electric2
EOQBronchoscope (Flexible Or Rigid)1
FBKEndoscopic Injection Needle, Gastroenterology-Urology1
FDXEndoscopic Cytology Brush1
FGEStents, Drains And Dilators For The Biliary Ducts1
KNSUnit, Electrosurgical, Endoscopic (With Or Without Accessories)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 23, 2008K083049TORNADO ROTATABEL SNARE AND POLYP CATCHER
Horizons Intl. Corp., CR
FDI
Oct 25, 2002K022268HORIZONS REUSABLE POLYPECTOMY SNARES
Horizons Intl. Corp.
FDI
Oct 25, 2002K022243HORIZONS REUSABLE HOT BIOPSY FORCEPS
Horizons Intl. Corp.
KGE
Aug 12, 2002K022546HORIZONS ANSO TRANSBRONCHIAL ASPIRATION NEEDLES
Horizons Intl. Corp.
EOQ
Jul 12, 2002K021998HORIZONS CYTOLOGY BRUSH
Horizons Intl. Corp.
FDX
Jun 21, 2002K021706HORIZONS HOT BIOPSY FORCEPS
Horizons Intl. Corp.
KGE
Aug 16, 2001K011667HORIZONS INTERNATIONAL POLYPECTOMY SNARES
Horizons Intl. Corp.
FDI
May 16, 2001K010448HORIZONS INTERNATIONAL VARICES INJECTION NEEDLES
Horizons Intl. Corp.
FBK
Jan 23, 2001K002236HORIZONS PAPILLOTOME
Horizons Intl. Corp.
KNS
Jan 23, 2001K002235HORIZONS ERCP CANNULA
Horizons Intl. Corp.
FGE

Latest recalls

DateFirm and productCodeLinked 510(k)
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