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CATHETER, DIGITAL POSITRAL II

Page Type
Cleared 510(K)
510(k) Number
K782082
510(k) Type
Traditional
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1978
Days to Decision
6 days

CATHETER, DIGITAL POSITRAL II

Page Type
Cleared 510(K)
510(k) Number
K782082
510(k) Type
Traditional
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1978
Days to Decision
6 days