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CIRCUFLOW 5208 SEQUENTIAL COMPRESSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K123647
510(k) Type
Traditional
Applicant
DEVON MEDICAL INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2013
Days to Decision
79 days
Submission Type
Summary

CIRCUFLOW 5208 SEQUENTIAL COMPRESSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K123647
510(k) Type
Traditional
Applicant
DEVON MEDICAL INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2013
Days to Decision
79 days
Submission Type
Summary