Last synced on 14 November 2025 at 11:06 pm

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)
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)
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