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MODEL 900S INTRAOCULAR PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812219
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1981
Days to Decision
102 days

MODEL 900S INTRAOCULAR PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812219
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1981
Days to Decision
102 days