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UROCOMP MODEL 1404

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K821939
510(k) Type
Traditional
Applicant
LIFE-TECH INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/1982
Days to Decision
14 days

UROCOMP MODEL 1404

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K821939
510(k) Type
Traditional
Applicant
LIFE-TECH INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/1982
Days to Decision
14 days