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Amplichek I, Negative , Amplichek I, Level 1, Amplichek I, Level 2, Amplichek I, Level 3, Amplichek I, MiniPak

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152679
510(k) Type
Traditional
Applicant
BIO-RAD LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2016
Days to Decision
235 days
Submission Type
Summary

Amplichek I, Negative , Amplichek I, Level 1, Amplichek I, Level 2, Amplichek I, Level 3, Amplichek I, MiniPak

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152679
510(k) Type
Traditional
Applicant
BIO-RAD LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2016
Days to Decision
235 days
Submission Type
Summary