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ANGIOGRAPHY NEEDLE W/WO CONNECTION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K840923
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/1984
Days to Decision
46 days

ANGIOGRAPHY NEEDLE W/WO CONNECTION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K840923
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/1984
Days to Decision
46 days