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IMMULITE MYOGLOBIN, MODEL LKMY1 AND LKMY5

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983970
510(k) Type
Traditional
Applicant
Diagnostic Products Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/1998
Days to Decision
16 days
Submission Type
Summary

IMMULITE MYOGLOBIN, MODEL LKMY1 AND LKMY5

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983970
510(k) Type
Traditional
Applicant
Diagnostic Products Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/1998
Days to Decision
16 days
Submission Type
Summary