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MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 33

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901638
510(k) Type
Traditional
Applicant
LASERMATIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1990
Days to Decision
79 days

MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 33

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901638
510(k) Type
Traditional
Applicant
LASERMATIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1990
Days to Decision
79 days