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TUBETECH IV Administration Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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