Last synced on 25 January 2026 at 3:41 am

LASER ASO KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K854039
510(k) Type
Traditional
Applicant
BEHRING DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1985
Days to Decision
26 days

LASER ASO KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K854039
510(k) Type
Traditional
Applicant
BEHRING DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1985
Days to Decision
26 days