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PNEUMOTHORAX KIT, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K904021
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/1990
Days to Decision
41 days

PNEUMOTHORAX KIT, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K904021
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/1990
Days to Decision
41 days