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MODEL 5050 SURGILASER FOR NEUROSURGERY USE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871933
510(k) Type
Traditional
Applicant
LASERMATIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1988
Days to Decision
248 days

MODEL 5050 SURGILASER FOR NEUROSURGERY USE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871933
510(k) Type
Traditional
Applicant
LASERMATIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1988
Days to Decision
248 days