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

Page Type
Cleared 510(K)
PDF
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
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