Last synced on 25 January 2026 at 3:41 am

SENSITITRE ARIS MODULE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911419
510(k) Type
Traditional
Applicant
SENSITITRE LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1992
Days to Decision
457 days

SENSITITRE ARIS MODULE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911419
510(k) Type
Traditional
Applicant
SENSITITRE LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1992
Days to Decision
457 days