Last synced on 14 November 2025 at 11:06 pm

ACUSON TRANSPERINEAL NEEDLE GUIDE

Page Type
Cleared 510(K)
510(k) Number
K874922
510(k) Type
Traditional
Applicant
ACUSON COMPUTED SONOGRAPHY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1988
Days to Decision
78 days

ACUSON TRANSPERINEAL NEEDLE GUIDE

Page Type
Cleared 510(K)
510(k) Number
K874922
510(k) Type
Traditional
Applicant
ACUSON COMPUTED SONOGRAPHY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1988
Days to Decision
78 days