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ACUSON TRANSRECTAL NEEDLE GUIDE FOR INTRA. APPLI.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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