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AIROS 8P Sequential Compression Device

Page Type
Cleared 510(K)
510(k) Number
K223193
510(k) Type
Traditional
Applicant
AIROS Medical, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2022
Days to Decision
57 days
Submission Type
Summary

AIROS 8P Sequential Compression Device

Page Type
Cleared 510(K)
510(k) Number
K223193
510(k) Type
Traditional
Applicant
AIROS Medical, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2022
Days to Decision
57 days
Submission Type
Summary