ClearanceBrief
Company ยท US

Circon Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1997 to 1999. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FASElectrode, Electrosurgical, Active, Urological1
GCXApparatus, Suction, Operating-Room, Wall Vacuum Powered1
HEWCuldoscope (And Accessories)1
HEXColposcope (And Colpomicroscope)1
KNFCoagulator-Cutter, Endoscopic, Unipolar (And Accessories)1
KNYAccessories, Catheter, G-U1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 26, 1999K992544TRANSVAGINAL HYDRO LAPAROSCOPY (THL) SYSTEM
Circon Corp.
HEX
Aug 3, 1999K992126CIRCON SURGIFLEX WAVE TSUNAMI SUCTION-IRRIGATION SYSTEM
Circon Corp.
GCX
Jul 30, 1998K981611SNAP-N-PEEL INTRODUCERS
Circon Corp.
KNY
Jun 12, 1998K980972RIGID CULDOSCOPE AND ACCESSORIES
Circon Corp.
HEW
May 12, 1998K973820USA ELITE SYSTEM VAPORTRODE VAPORIZATION ELECTRODE AND VAPORTOME RESECTION ELECTRODE
Circon Corp.
FAS
Aug 15, 1997K964594VAPORTRODE VAPORIZATION ELECTRODE -GROOVED/FLUTED/SPIKED(GVE-B,GVE-F,GVE-S) & VAPORTOMME VAPORIZATION LOOP (GVE-LG)
Circon Corp.
KNF

Latest recalls

DateFirm and productCodeLinked 510(k)
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