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Biotrax, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K904496 CROMATEST SYPHILIS DIAGNOSTICGMQ1991-07-24 View
510(k) K904416 CROATEST (R) RHEUMATOID DIAGNOSTICGTQ1991-06-24 View
510(k) K904497 CROMATEST RHEUMATOID DIAGNOSTIC/CRP LATEX TESTDCN1990-11-01 View
510(k) K904498 CROMATEST RHEUMATOID DIAGNOSTIC/RF LATEX TESTDHR1990-10-29 View
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