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INTERLINK(TM) BLUNT CANNULA, MODIFICATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911868
510(k) Type
Traditional
Applicant
BAXTER HEALTHCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1991
Days to Decision
59 days
Submission Type
Statement

INTERLINK(TM) BLUNT CANNULA, MODIFICATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911868
510(k) Type
Traditional
Applicant
BAXTER HEALTHCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1991
Days to Decision
59 days
Submission Type
Statement