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CATHETER WITH GUIDEWIRE ASSEMBLY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K900056
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1990
Days to Decision
224 days

CATHETER WITH GUIDEWIRE ASSEMBLY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K900056
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1990
Days to Decision
224 days