Last synced on 6 June 2025 at 11:06 pm

RANDOX FERRITIN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000662
510(k) Type
Traditional
Applicant
RANDOX LABORATORIES, LTD.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
4/3/2000
Days to Decision
35 days
Submission Type
Statement

RANDOX FERRITIN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000662
510(k) Type
Traditional
Applicant
RANDOX LABORATORIES, LTD.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
4/3/2000
Days to Decision
35 days
Submission Type
Statement