Last synced on 14 November 2025 at 11:06 pm

OSOM HCG COMBO TEST

Page Type
Cleared 510(K)
510(k) Number
K955141
510(k) Type
Traditional
Applicant
WYNTEK DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/1995
Days to Decision
23 days
Submission Type
Summary

OSOM HCG COMBO TEST

Page Type
Cleared 510(K)
510(k) Number
K955141
510(k) Type
Traditional
Applicant
WYNTEK DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/1995
Days to Decision
23 days
Submission Type
Summary