Last synced on 18 April 2025 at 11:05 pm

SENTRY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K792653
510(k) Type
Traditional
Applicant
AUTOMATED SCREENING DEVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/1980
Days to Decision
9 days

SENTRY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K792653
510(k) Type
Traditional
Applicant
AUTOMATED SCREENING DEVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/1980
Days to Decision
9 days