Wyntek Diagnostics, Inc.
Wyntek Diagnostics, Inc. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 2000.
Top product codes for Wyntek Diagnostics, Inc.
Recent clearances by Wyntek Diagnostics, Inc.
- K992658 — OSOM ULTRA STREP A TEST, MODEL 147
- K990576 — OSOM CARD PREGNANCY TEST, MODEL 103
- K990578 — OSOM CARD II HCG-URINE TEST, MODEL 102
- K974159 — OSOM HCG-URINE TEST MODEL 101
- K973879 — OSOM CARD HCG-URINE TEST
- K972231 — OSOM MONO TEST 143
- K965184 — PERFECTA PREGNANCY TEST
- K965227 — OSOM CLASSIC HCG-URINE TEST (115)
- K961423 — OSOM STREP A TEST
- K955141 — OSOM HCG COMBO TEST
- K954178 — OSOM PREGNANCY TEST
- K953383 — WYNTEK OSOM HCG-URINE TEST
Data sourced from openFDA. This site is unofficial and independent of the FDA.