Last synced on 20 June 2025 at 11:06 pm

IMMULITE C-REACTIVE PROTEIN, MODEL LKCR1, LKCR5

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990886
510(k) Type
Special
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1999
Days to Decision
20 days
Submission Type
Summary

IMMULITE C-REACTIVE PROTEIN, MODEL LKCR1, LKCR5

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990886
510(k) Type
Special
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1999
Days to Decision
20 days
Submission Type
Summary