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MCCARTNEY ACCESS TUBE

Page Type
Cleared 510(K)
510(k) Number
K051594
510(k) Type
Traditional
Applicant
GYNETECH PTY. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2005
Days to Decision
78 days
Submission Type
Summary

MCCARTNEY ACCESS TUBE

Page Type
Cleared 510(K)
510(k) Number
K051594
510(k) Type
Traditional
Applicant
GYNETECH PTY. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2005
Days to Decision
78 days
Submission Type
Summary