Last synced on 14 November 2025 at 11:06 pm

CURAE'LASE CL1000 IR LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K053201
510(k) Type
Traditional
Applicant
CURAE'LASE INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2005
Days to Decision
23 days
Submission Type
Summary

CURAE'LASE CL1000 IR LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K053201
510(k) Type
Traditional
Applicant
CURAE'LASE INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2005
Days to Decision
23 days
Submission Type
Summary