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PATHFINDER(TM) CHLAMYDIA EIA DETECT KIT/MODIFIED

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884517
510(k) Type
Traditional
Applicant
KALLESTAD DIAG, A DIV. OF ERBAMONT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/1988
Days to Decision
34 days

PATHFINDER(TM) CHLAMYDIA EIA DETECT KIT/MODIFIED

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884517
510(k) Type
Traditional
Applicant
KALLESTAD DIAG, A DIV. OF ERBAMONT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/1988
Days to Decision
34 days