Circon Corp.

FDA Regulatory Profile

Circon Corp. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 26, 1999.

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K992544TRANSVAGINAL HYDRO LAPAROSCOPY (THL) SYSTEMOctober 26, 1999
K992126CIRCON SURGIFLEX WAVE TSUNAMI SUCTION-IRRIGATION SYSTEMAugust 3, 1999
K981611SNAP-N-PEEL INTRODUCERSJuly 30, 1998
K980972RIGID CULDOSCOPE AND ACCESSORIESJune 12, 1998
K973820USA ELITE SYSTEM VAPORTRODE VAPORIZATION ELECTRODE AND VAPORTOME RESECTION ELECTRODEMay 12, 1998
K964594VAPORTRODE VAPORIZATION ELECTRODE -GROOVED/FLUTED/SPIKED(GVE-B,GVE-F,GVE-S) & VAPORTOMME VAPORIZATIOAugust 15, 1997