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P51 ANGIOPLASTY PRESSURE TRANSDUCER

Page Type
Cleared 510(K)
510(k) Number
K813331
510(k) Type
Traditional
Applicant
KONIGSBERG INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1981
Days to Decision
35 days

P51 ANGIOPLASTY PRESSURE TRANSDUCER

Page Type
Cleared 510(K)
510(k) Number
K813331
510(k) Type
Traditional
Applicant
KONIGSBERG INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1981
Days to Decision
35 days