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Surgi-Vision, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K111073SURGIVISION INC. CLEARPOINT SYSTEMJune 22, 2011
K020790INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL MICROCOIL, AND INTERCEPT VASCULAR INTERNALMay 21, 2002
K020495INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL INTERNAL MR COIL, AND INTERCEPT VASCULAR IApril 23, 2002
K011781INTERCEPT-URETHRAL MICROCOILAugust 31, 2001
K003436SURGI-VISION GUIDEWIRE COILFebruary 2, 2001
K002916SURGI-VISION PROSTATE COILNovember 28, 2000
K002345SURGI-VISION URETHRAL COILOctober 11, 2000
K994436SURGI-VISION ESOPHAGEAL STYLET COILMarch 14, 2000
K992193ENDO-ESOPHAGEAL MR COILSeptember 3, 1999