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TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940203
510(k) Type
Traditional
Applicant
LIFE-TECH INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/1994
Days to Decision
76 days
Submission Type
Statement

TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940203
510(k) Type
Traditional
Applicant
LIFE-TECH INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/1994
Days to Decision
76 days
Submission Type
Statement