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CATHETER TWO STAGE VENOUS RETURN

Page Type
Cleared 510(K)
510(k) Number
K915268
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1992
Days to Decision
245 days
Submission Type
Statement

CATHETER TWO STAGE VENOUS RETURN

Page Type
Cleared 510(K)
510(k) Number
K915268
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1992
Days to Decision
245 days
Submission Type
Statement