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CARDIOLIPIN IGG,M,A EIA TEST KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952520
510(k) Type
Traditional
Applicant
IMMUNO PROBE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1995
Days to Decision
106 days
Submission Type
Summary

CARDIOLIPIN IGG,M,A EIA TEST KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952520
510(k) Type
Traditional
Applicant
IMMUNO PROBE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1995
Days to Decision
106 days
Submission Type
Summary