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LH GEN III SELF-TEST/CONCEIVE

Page Type
Cleared 510(K)
510(k) Number
K920160
510(k) Type
Traditional
Applicant
QUIDEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1992
Days to Decision
57 days
Submission Type
Summary

LH GEN III SELF-TEST/CONCEIVE

Page Type
Cleared 510(K)
510(k) Number
K920160
510(k) Type
Traditional
Applicant
QUIDEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1992
Days to Decision
57 days
Submission Type
Summary