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CEDIA Buprenorphine II Assay; CEDIA Buprenorphine II Calibrators; CEDIA Negative Calibrator II; CEDIA Buprenorphine II Control Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163101
510(k) Type
Traditional
Applicant
MICROGENICS CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2017
Days to Decision
150 days
Submission Type
Summary

CEDIA Buprenorphine II Assay; CEDIA Buprenorphine II Calibrators; CEDIA Negative Calibrator II; CEDIA Buprenorphine II Control Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163101
510(k) Type
Traditional
Applicant
MICROGENICS CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2017
Days to Decision
150 days
Submission Type
Summary