Last synced on 11 July 2025 at 11:06 pm

DIATEK CANNON-CATH #CC2400, CC2800, CC3200, CC3600,CC5500. CC2400PC, CC2800PC, CC3200PC(32 CM), CC3200PC(36 CM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010399
510(k) Type
Traditional
Applicant
DIATEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2001
Days to Decision
186 days
Submission Type
Summary

DIATEK CANNON-CATH #CC2400, CC2800, CC3200, CC3600,CC5500. CC2400PC, CC2800PC, CC3200PC(32 CM), CC3200PC(36 CM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010399
510(k) Type
Traditional
Applicant
DIATEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2001
Days to Decision
186 days
Submission Type
Summary