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ESENSOR CYSTIC FIBROSIS CARRIER DETECTION TEST , ESENSOR 4800 DNA DETECTION SYSTEM, MODEL 4800

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051435
510(k) Type
Traditional
Applicant
Clinical Micro Sensors
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2006
Days to Decision
232 days
Submission Type
Summary

ESENSOR CYSTIC FIBROSIS CARRIER DETECTION TEST , ESENSOR 4800 DNA DETECTION SYSTEM, MODEL 4800

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051435
510(k) Type
Traditional
Applicant
Clinical Micro Sensors
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2006
Days to Decision
232 days
Submission Type
Summary