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LOS 3D VISION 100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953419
510(k) Type
Traditional
Applicant
LASER OPTIK SYSTEME GMBH & CO. KG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/8/1996
Days to Decision
220 days
Submission Type
Statement