Last synced on 30 May 2025 at 11:05 pm

DIRECT TIBC KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000781
510(k) Type
Traditional
Applicant
REFERENCE DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2000
Days to Decision
53 days
Submission Type
Statement

DIRECT TIBC KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000781
510(k) Type
Traditional
Applicant
REFERENCE DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2000
Days to Decision
53 days
Submission Type
Statement