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CLEARLINK ANTIMICROBIAL LUER ACTIVATED DEVICE (LAD) AND EXTENSION SETS WITH THE CLEARLINK ANTIMICROBIAL LUER ACTIVATED

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072576
510(k) Type
Traditional
Applicant
Baxter Healthcare Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/2007
Days to Decision
54 days
Submission Type
Summary

CLEARLINK ANTIMICROBIAL LUER ACTIVATED DEVICE (LAD) AND EXTENSION SETS WITH THE CLEARLINK ANTIMICROBIAL LUER ACTIVATED

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072576
510(k) Type
Traditional
Applicant
Baxter Healthcare Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/2007
Days to Decision
54 days
Submission Type
Summary