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WECK REUSABLE OBTURATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121796
510(k) Type
Traditional
Applicant
Teleflexmedical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2012
Days to Decision
114 days
Submission Type
Summary

WECK REUSABLE OBTURATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121796
510(k) Type
Traditional
Applicant
Teleflexmedical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2012
Days to Decision
114 days
Submission Type
Summary