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NEUTRAL LUER ACTIVATED DEVICE AND EXTENSION SETS WITH NEUTRAL LUER ACTIVATED DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120443
510(k) Type
Traditional
Applicant
Baxter Healthcare Corporation - Renal Division
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2012
Days to Decision
98 days
Submission Type
Summary

NEUTRAL LUER ACTIVATED DEVICE AND EXTENSION SETS WITH NEUTRAL LUER ACTIVATED DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120443
510(k) Type
Traditional
Applicant
Baxter Healthcare Corporation - Renal Division
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2012
Days to Decision
98 days
Submission Type
Summary