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PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K072372
510(k) Type
Traditional
Applicant
MEGO AFEK
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
11/21/2007
Days to Decision
90 days
Submission Type
Summary

PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K072372
510(k) Type
Traditional
Applicant
MEGO AFEK
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
11/21/2007
Days to Decision
90 days
Submission Type
Summary