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ARGYLE PERIPHERALLY INSERTED CENTRAL CATHETER SINGLE LUMEN, ARGYLE PERIPHERALLY INSERTED CENTRAL CATHETER DUAL LUMEN

Page Type
Cleared 510(K)
510(k) Number
K132567
510(k) Type
Special
Applicant
COVIDIEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2013
Days to Decision
82 days
Submission Type
Summary

ARGYLE PERIPHERALLY INSERTED CENTRAL CATHETER SINGLE LUMEN, ARGYLE PERIPHERALLY INSERTED CENTRAL CATHETER DUAL LUMEN

Page Type
Cleared 510(K)
510(k) Number
K132567
510(k) Type
Special
Applicant
COVIDIEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2013
Days to Decision
82 days
Submission Type
Summary