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Helios III

Page Type
Cleared 510(K)
510(k) Number
K152856
510(k) Type
Traditional
Applicant
LASEROPTEK CO. LTD.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
6/2/2016
Days to Decision
247 days
Submission Type
Summary

Helios III

Page Type
Cleared 510(K)
510(k) Number
K152856
510(k) Type
Traditional
Applicant
LASEROPTEK CO. LTD.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
6/2/2016
Days to Decision
247 days
Submission Type
Summary