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STERILE CHEST TUBE

Page Type
Cleared 510(K)
510(k) Number
K913733
510(k) Type
Traditional
Applicant
VASCULAR PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/1991
Days to Decision
49 days
Submission Type
Statement

STERILE CHEST TUBE

Page Type
Cleared 510(K)
510(k) Number
K913733
510(k) Type
Traditional
Applicant
VASCULAR PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/1991
Days to Decision
49 days
Submission Type
Statement