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MODEL 4900 ND:YAG LASER FOR NEUROSURGERY APPLICA.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880172
510(k) Type
Traditional
Applicant
COOPER LASERSONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1988
Days to Decision
56 days

MODEL 4900 ND:YAG LASER FOR NEUROSURGERY APPLICA.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880172
510(k) Type
Traditional
Applicant
COOPER LASERSONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1988
Days to Decision
56 days