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SINGLE SITE FLEXIBLE BLADELESS OBTURATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101671
510(k) Type
Special
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/2010
Days to Decision
11 days
Submission Type
Summary