Last synced on 23 September 2022 at 11:05 pm

AMERLITE MAB FT4 ASSAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K955097
510(k) Type
Traditional
Applicant
KODAK CLINICAL DIAGNOSTICS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/20/1995
Days to Decision
43 days
Submission Type
Statement

AMERLITE MAB FT4 ASSAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K955097
510(k) Type
Traditional
Applicant
KODAK CLINICAL DIAGNOSTICS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/20/1995
Days to Decision
43 days
Submission Type
Statement