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BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874618
510(k) Type
Traditional
Applicant
BENTLEY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1988
Days to Decision
71 days

BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874618
510(k) Type
Traditional
Applicant
BENTLEY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1988
Days to Decision
71 days