Last synced on 25 January 2026 at 3:41 am

RUBELLA IGG ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM IN-VITRO DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951359
510(k) Type
Traditional
Applicant
Bayer Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/1996
Days to Decision
385 days
Submission Type
Summary

RUBELLA IGG ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM IN-VITRO DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951359
510(k) Type
Traditional
Applicant
Bayer Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/1996
Days to Decision
385 days
Submission Type
Summary