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NUVOLASE 532 LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K990725
510(k) Type
Special
Applicant
AMERICAN LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1999
Days to Decision
17 days
Submission Type
Summary

NUVOLASE 532 LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K990725
510(k) Type
Special
Applicant
AMERICAN LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1999
Days to Decision
17 days
Submission Type
Summary