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LOTUS II PULSED ER: YAG LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083253
510(k) Type
Traditional
Applicant
LASEROPTEK CO. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2009
Days to Decision
192 days
Submission Type
Summary

LOTUS II PULSED ER: YAG LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083253
510(k) Type
Traditional
Applicant
LASEROPTEK CO. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2009
Days to Decision
192 days
Submission Type
Summary