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INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL INTERNAL MR COIL, AND INTERCEPT VASCULAR INTERNAL MR COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020495
510(k) Type
Traditional
Applicant
SURGI-VISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/2002
Days to Decision
68 days
Submission Type
Summary

INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL INTERNAL MR COIL, AND INTERCEPT VASCULAR INTERNAL MR COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020495
510(k) Type
Traditional
Applicant
SURGI-VISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/2002
Days to Decision
68 days
Submission Type
Summary