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FLUOBEAM 800 CLINIC LASER IMAGING DEVICE AND FLUOCASE 800 CONTROL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132475
510(k) Type
Traditional
Applicant
FLUOPTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/2014
Days to Decision
273 days
Submission Type
Summary

FLUOBEAM 800 CLINIC LASER IMAGING DEVICE AND FLUOCASE 800 CONTROL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132475
510(k) Type
Traditional
Applicant
FLUOPTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/2014
Days to Decision
273 days
Submission Type
Summary