Last synced on 14 November 2025 at 11:06 pm

Aurolase Therapy, Laser Delivery Device (LDD)

Page Type
Cleared 510(K)
510(k) Number
K202953
510(k) Type
Traditional
Applicant
Nanospectra Biosciences, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2022
Days to Decision
733 days
Submission Type
Summary

Aurolase Therapy, Laser Delivery Device (LDD)

Page Type
Cleared 510(K)
510(k) Number
K202953
510(k) Type
Traditional
Applicant
Nanospectra Biosciences, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2022
Days to Decision
733 days
Submission Type
Summary