Last synced on 2 May 2025 at 11:05 pm

QUICK-CLIP NEEDLE GUIDE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903561
510(k) Type
Traditional
Applicant
ACUSON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1991
Days to Decision
210 days

QUICK-CLIP NEEDLE GUIDE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903561
510(k) Type
Traditional
Applicant
ACUSON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1991
Days to Decision
210 days