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SINGLE SITE FLEXIBLE BLADELESS OBTURATOR

Page Type
Cleared 510(K)
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

SINGLE SITE FLEXIBLE BLADELESS OBTURATOR

Page Type
Cleared 510(K)
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