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RANDOX PHENYTOIN

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011393
510(k) Type
Traditional
Applicant
Randox Laboratories, Ltd.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
12/4/2001
Days to Decision
211 days
Submission Type
Statement

RANDOX PHENYTOIN

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011393
510(k) Type
Traditional
Applicant
Randox Laboratories, Ltd.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
12/4/2001
Days to Decision
211 days
Submission Type
Statement