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ADMS TRANSRECTAL 7.5 MHZ PROBE

Page Type
Cleared 510(K)
510(k) Number
K870967
510(k) Type
Traditional
Applicant
DIASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1987
Days to Decision
203 days

ADMS TRANSRECTAL 7.5 MHZ PROBE

Page Type
Cleared 510(K)
510(k) Number
K870967
510(k) Type
Traditional
Applicant
DIASONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1987
Days to Decision
203 days