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OPTILOCK IMPLANTABLE ACCESS PORT, MODEL 1700-05

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031282
510(k) Type
Traditional
Applicant
LEMAITRE VASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2003
Days to Decision
105 days
Submission Type
Statement

OPTILOCK IMPLANTABLE ACCESS PORT, MODEL 1700-05

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031282
510(k) Type
Traditional
Applicant
LEMAITRE VASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2003
Days to Decision
105 days
Submission Type
Statement