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Lustre PRO Light System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143713
510(k) Type
Traditional
Applicant
AMBICARE HEALTH LTD
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/19/2016
Days to Decision
386 days
Submission Type
Summary

Lustre PRO Light System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143713
510(k) Type
Traditional
Applicant
AMBICARE HEALTH LTD
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/19/2016
Days to Decision
386 days
Submission Type
Summary