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IMMULITE ANTI-TPO-AB(LKTOI,LKT05,LKTOZ

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963695
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1997
Days to Decision
123 days
Submission Type
Summary

IMMULITE ANTI-TPO-AB(LKTOI,LKT05,LKTOZ

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963695
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1997
Days to Decision
123 days
Submission Type
Summary