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MAXReach Laser Probe

Page Type
Cleared 510(K)
510(k) Number
K191846
510(k) Type
Traditional
Applicant
Vortex Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2019
Days to Decision
166 days
Submission Type
Summary

MAXReach Laser Probe

Page Type
Cleared 510(K)
510(k) Number
K191846
510(k) Type
Traditional
Applicant
Vortex Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2019
Days to Decision
166 days
Submission Type
Summary