Last synced on 11 July 2025 at 11:06 pm

MODIFIED FERRITIN ENZYME IMMUNOASSAY TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896585
510(k) Type
Traditional
Applicant
MEDIX BIOTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1989
Days to Decision
13 days

MODIFIED FERRITIN ENZYME IMMUNOASSAY TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896585
510(k) Type
Traditional
Applicant
MEDIX BIOTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1989
Days to Decision
13 days