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LARS AC Band Device

Page Type
Cleared 510(K)
510(k) Number
K190143
510(k) Type
Traditional
Applicant
Corin USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/2019
Days to Decision
279 days
Submission Type
Summary

LARS AC Band Device

Page Type
Cleared 510(K)
510(k) Number
K190143
510(k) Type
Traditional
Applicant
Corin USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/2019
Days to Decision
279 days
Submission Type
Summary