Last synced on 25 January 2026 at 3:41 am

ACTILLUME

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894044
510(k) Type
Traditional
Applicant
AMBULATORY MONITORING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1989
Days to Decision
198 days

ACTILLUME

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894044
510(k) Type
Traditional
Applicant
AMBULATORY MONITORING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1989
Days to Decision
198 days