Last synced on 25 January 2026 at 3:41 am

COULTER AC.T SERIES ANALYZER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964988
510(k) Type
Traditional
Applicant
Coulter Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1997
Days to Decision
83 days
Submission Type
Summary

COULTER AC.T SERIES ANALYZER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964988
510(k) Type
Traditional
Applicant
Coulter Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1997
Days to Decision
83 days
Submission Type
Summary