Last synced on 25 January 2026 at 3:41 am

T UPTAKE ENZYME IMMUNOASSAY CRIMPED TUBE KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896925
510(k) Type
Traditional
Applicant
IN VITRO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1990
Days to Decision
37 days

T UPTAKE ENZYME IMMUNOASSAY CRIMPED TUBE KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896925
510(k) Type
Traditional
Applicant
IN VITRO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1990
Days to Decision
37 days