Last synced on 25 April 2025 at 11:05 pm

NUVOLASE 532 CUTANEOUS LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990780
510(k) Type
Special
Applicant
AMERICAN LASER MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1999
Days to Decision
13 days
Submission Type
Summary

NUVOLASE 532 CUTANEOUS LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990780
510(k) Type
Special
Applicant
AMERICAN LASER MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1999
Days to Decision
13 days
Submission Type
Summary