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

Page Type
Cleared 510(K)
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)
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