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LUTEINIZING HORMONE RADIOIMMUNOASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K803278
510(k) Type
Traditional
Applicant
IMMUNO NUCLEAR CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/1981
Days to Decision
23 days

LUTEINIZING HORMONE RADIOIMMUNOASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K803278
510(k) Type
Traditional
Applicant
IMMUNO NUCLEAR CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/1981
Days to Decision
23 days