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TUBETECH IV Administration Set

Page Type
Cleared 510(K)
510(k) Number
K162951
510(k) Type
Traditional
Applicant
Douglas Medical Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2017
Days to Decision
277 days
Submission Type
Statement

TUBETECH IV Administration Set

Page Type
Cleared 510(K)
510(k) Number
K162951
510(k) Type
Traditional
Applicant
Douglas Medical Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2017
Days to Decision
277 days
Submission Type
Statement