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Emit II Plus Buprenorphine Assay, Emit II Plus Specialty Drug Calibrator/Control Level 1, Level 2 Level 3, Level 4, Emit II Plus Specialty Drug Control Negative, Emit II Plus Specialty Drug Control Positive

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150606
510(k) Type
Traditional
Applicant
Siemens Healthcare Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/2015
Days to Decision
227 days
Submission Type
Summary

Emit II Plus Buprenorphine Assay, Emit II Plus Specialty Drug Calibrator/Control Level 1, Level 2 Level 3, Level 4, Emit II Plus Specialty Drug Control Negative, Emit II Plus Specialty Drug Control Positive

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150606
510(k) Type
Traditional
Applicant
Siemens Healthcare Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/2015
Days to Decision
227 days
Submission Type
Summary