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SEROLISA CHLAMYDIA IGG TEST KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915281
510(k) Type
Traditional
Applicant
SAVYON DIAGNOSTICS, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
3/23/1992
Days to Decision
119 days
Submission Type
Summary

SEROLISA CHLAMYDIA IGG TEST KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915281
510(k) Type
Traditional
Applicant
SAVYON DIAGNOSTICS, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
3/23/1992
Days to Decision
119 days
Submission Type
Summary