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MANIPULATOR; MANIPULATOR PRO

Page Type
Cleared 510(K)
510(k) Number
K142164
510(k) Type
Traditional
Applicant
GYNETECH PTY. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2014
Days to Decision
133 days
Submission Type
Summary

MANIPULATOR; MANIPULATOR PRO

Page Type
Cleared 510(K)
510(k) Number
K142164
510(k) Type
Traditional
Applicant
GYNETECH PTY. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2014
Days to Decision
133 days
Submission Type
Summary