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DESERET ANGIO-GUIDE LARGE VEIN CATH.

Page Type
Cleared 510(K)
510(k) Number
K833092
510(k) Type
Traditional
Applicant
WARNER-LAMBERT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1983
Days to Decision
70 days

DESERET ANGIO-GUIDE LARGE VEIN CATH.

Page Type
Cleared 510(K)
510(k) Number
K833092
510(k) Type
Traditional
Applicant
WARNER-LAMBERT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1983
Days to Decision
70 days