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ELISA TUBE LH TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K920920
510(k) Type
Traditional
Applicant
BIO CLINIC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/1992
Days to Decision
40 days
Submission Type
Statement

ELISA TUBE LH TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K920920
510(k) Type
Traditional
Applicant
BIO CLINIC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/1992
Days to Decision
40 days
Submission Type
Statement