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SMARTRION COMBI/Alexandrite & Long Pulsed Nd:YAG Laser

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222485
510(k) Type
Traditional
Applicant
IDS, Limited
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
3/29/2023
Days to Decision
224 days
Submission Type
Statement

SMARTRION COMBI/Alexandrite & Long Pulsed Nd:YAG Laser

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222485
510(k) Type
Traditional
Applicant
IDS, Limited
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
3/29/2023
Days to Decision
224 days
Submission Type
Statement