Last synced on 25 January 2026 at 3:41 am

VIS-CUBE PREGNANCY HOME TEST,CAT. # JPL-042

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K863999
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1987
Days to Decision
87 days

VIS-CUBE PREGNANCY HOME TEST,CAT. # JPL-042

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K863999
510(k) Type
Traditional
Applicant
LEECO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1987
Days to Decision
87 days