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LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM

Page Type
Cleared 510(K)
510(k) Number
K052797
510(k) Type
Traditional
Applicant
MEDTEK DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2006
Days to Decision
133 days
Submission Type
Summary

LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM

Page Type
Cleared 510(K)
510(k) Number
K052797
510(k) Type
Traditional
Applicant
MEDTEK DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2006
Days to Decision
133 days
Submission Type
Summary