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QUANTA Flash® LKM-1 Reagents, QUANTA Flash® LKM-1 Calibrators, QUANTA Flash® LKM-1 Controls

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163538
510(k) Type
Traditional
Applicant
Inova Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2017
Days to Decision
264 days
Submission Type
Summary

QUANTA Flash® LKM-1 Reagents, QUANTA Flash® LKM-1 Calibrators, QUANTA Flash® LKM-1 Controls

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163538
510(k) Type
Traditional
Applicant
Inova Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2017
Days to Decision
264 days
Submission Type
Summary