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LYMPHA PRESS PLUS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K013331
510(k) Type
Traditional
Applicant
MEGO AFEK
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
11/30/2001
Days to Decision
56 days
Submission Type
Summary

LYMPHA PRESS PLUS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K013331
510(k) Type
Traditional
Applicant
MEGO AFEK
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
11/30/2001
Days to Decision
56 days
Submission Type
Summary