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LUX-Dx II (M302); LUX-Dx II+ (M312)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231328
510(k) Type
Traditional
Applicant
Boston Scientific Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2023
Days to Decision
103 days
Submission Type
Summary

LUX-Dx II (M302); LUX-Dx II+ (M312)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231328
510(k) Type
Traditional
Applicant
Boston Scientific Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2023
Days to Decision
103 days
Submission Type
Summary