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ACUSON TRANSRECTAL NEEDLE GUIDE FOR INTRA. APPLI.

Page Type
Cleared 510(K)
510(k) Number
K882549
510(k) Type
Traditional
Applicant
ACUSON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/1988
Days to Decision
31 days

ACUSON TRANSRECTAL NEEDLE GUIDE FOR INTRA. APPLI.

Page Type
Cleared 510(K)
510(k) Number
K882549
510(k) Type
Traditional
Applicant
ACUSON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/1988
Days to Decision
31 days