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O-pel Laser and families of probe delivery devices

Page Type
Cleared 510(K)
510(k) Number
K160012
510(k) Type
Traditional
Applicant
PRECISE LIGHT SURGICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2016
Days to Decision
150 days
Submission Type
Summary

O-pel Laser and families of probe delivery devices

Page Type
Cleared 510(K)
510(k) Number
K160012
510(k) Type
Traditional
Applicant
PRECISE LIGHT SURGICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2016
Days to Decision
150 days
Submission Type
Summary