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InsufflatOR Needle

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142700
510(k) Type
Traditional
Applicant
GYNETECH PTY. LTD.
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
12/19/2014
Days to Decision
88 days
Submission Type
Summary

InsufflatOR Needle

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142700
510(k) Type
Traditional
Applicant
GYNETECH PTY. LTD.
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
12/19/2014
Days to Decision
88 days
Submission Type
Summary