Last synced on 27 January 2023 at 11:04 pm

OVUQUICK SELF-TEST (OVUQUICK; RAMP LH ASSAY)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871726
510(k) Type
Traditional
Applicant
MONOCLONAL ANTIBODIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1987
Days to Decision
83 days

OVUQUICK SELF-TEST (OVUQUICK; RAMP LH ASSAY)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871726
510(k) Type
Traditional
Applicant
MONOCLONAL ANTIBODIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1987
Days to Decision
83 days