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INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL MICROCOIL, 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
K020790
510(k) Type
Traditional
Applicant
SURGI-VISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2002
Days to Decision
71 days
Submission Type
Summary

INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL MICROCOIL, 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
K020790
510(k) Type
Traditional
Applicant
SURGI-VISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2002
Days to Decision
71 days
Submission Type
Summary