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Randox RX Daytona Plus Magnesium (MG)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162200
510(k) Type
Traditional
Applicant
Randox Laboratories, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/28/2017
Days to Decision
266 days
Submission Type
Summary

Randox RX Daytona Plus Magnesium (MG)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162200
510(k) Type
Traditional
Applicant
Randox Laboratories, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/28/2017
Days to Decision
266 days
Submission Type
Summary