Last synced on 25 January 2026 at 3:41 am

SELF ASSURE/GHB (CAPILLARY-BLOOD COLLECTION KIT)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861697
510(k) Type
Traditional
Applicant
AWARENESS TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/1986
Days to Decision
106 days

SELF ASSURE/GHB (CAPILLARY-BLOOD COLLECTION KIT)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861697
510(k) Type
Traditional
Applicant
AWARENESS TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/1986
Days to Decision
106 days