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MDLS 4000/4900/6000/8000/8900/LUXUS 60/100 ND:YAG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903444
510(k) Type
Traditional
Applicant
HERAEUS LASERSONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/1990
Days to Decision
76 days

MDLS 4000/4900/6000/8000/8900/LUXUS 60/100 ND:YAG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903444
510(k) Type
Traditional
Applicant
HERAEUS LASERSONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/1990
Days to Decision
76 days