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ARTERIOFLOW MODEL 7500 SEQUENTIAL COMPRESSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K102582
510(k) Type
Traditional
Applicant
DEVON MEDICAL INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2010
Days to Decision
29 days
Submission Type
Summary

ARTERIOFLOW MODEL 7500 SEQUENTIAL COMPRESSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K102582
510(k) Type
Traditional
Applicant
DEVON MEDICAL INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2010
Days to Decision
29 days
Submission Type
Summary