Last synced on 25 January 2026 at 3:41 am

GUIDEWIRE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890959
510(k) Type
Traditional
Applicant
GUIDEWIRE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/1989
Days to Decision
197 days

GUIDEWIRE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890959
510(k) Type
Traditional
Applicant
GUIDEWIRE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/1989
Days to Decision
197 days