Last synced on 27 June 2025 at 11:06 pm

NUCLISENS EASYQ ENTEROVIRUS V1.1., NUCLISENS EASYQ DIRECTOR 2.6, NUCLISENS EASYQ ANALYZER, NUCLISENS MINIMAG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093383
510(k) Type
Traditional
Applicant
BIOMERIEUX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2010
Days to Decision
249 days
Submission Type
Summary

NUCLISENS EASYQ ENTEROVIRUS V1.1., NUCLISENS EASYQ DIRECTOR 2.6, NUCLISENS EASYQ ANALYZER, NUCLISENS MINIMAG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093383
510(k) Type
Traditional
Applicant
BIOMERIEUX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2010
Days to Decision
249 days
Submission Type
Summary