Last synced on 23 September 2022 at 11:05 pm

ManipulatOR PRO, ManipulatOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150519
510(k) Type
Traditional
Applicant
GYNETECH PTY. LTD.
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
8/19/2015
Days to Decision
170 days
Submission Type
Summary

ManipulatOR PRO, ManipulatOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150519
510(k) Type
Traditional
Applicant
GYNETECH PTY. LTD.
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
8/19/2015
Days to Decision
170 days
Submission Type
Summary