Last synced on 30 September 2022 at 11:05 pm

MANIPULATOR; MANIPULATOR PRO

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