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MODELS 4000/6000/8000/8900 LASER FOR DERMA/SURGERY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K873790
510(k) Type
Traditional
Applicant
COOPER LASERSONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1988
Days to Decision
126 days

MODELS 4000/6000/8000/8900 LASER FOR DERMA/SURGERY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K873790
510(k) Type
Traditional
Applicant
COOPER LASERSONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1988
Days to Decision
126 days