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LUTEINIZING HORMONE RADIOIMMUNOASSAY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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