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HELIOS IV 785

Page Type
Cleared 510(K)
510(k) Number
K212663
510(k) Type
Traditional
Applicant
Laseroptek Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
6/9/2022
Days to Decision
290 days
Submission Type
Summary

HELIOS IV 785

Page Type
Cleared 510(K)
510(k) Number
K212663
510(k) Type
Traditional
Applicant
Laseroptek Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
6/9/2022
Days to Decision
290 days
Submission Type
Summary