Last synced on 25 January 2026 at 3:41 am

ROTACLONE ROTAVIRUS DIAGNOSTIC KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852969
510(k) Type
Traditional
Applicant
CAMBRIDGE BIOSCIENCE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1985
Days to Decision
113 days

ROTACLONE ROTAVIRUS DIAGNOSTIC KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852969
510(k) Type
Traditional
Applicant
CAMBRIDGE BIOSCIENCE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1985
Days to Decision
113 days