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SOFTECH PLUS ETC02 CANNULA

Page Type
Cleared 510(K)
510(k) Number
K132946
510(k) Type
Traditional
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2014
Days to Decision
258 days
Submission Type
Summary

SOFTECH PLUS ETC02 CANNULA

Page Type
Cleared 510(K)
510(k) Number
K132946
510(k) Type
Traditional
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2014
Days to Decision
258 days
Submission Type
Summary