Sweden Diagnostics (Germany) GmbH
Sweden Diagnostics (Germany) GmbH holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2005.
Top product codes for Sweden Diagnostics (Germany) GmbH
Recent clearances by Sweden Diagnostics (Germany) GmbH
- K050967 — VARELISA RECOMBI CTD SCREEN, MODEL 13096
- K050625 — VARELISA RECOMBI ANA PROFILE, MODEL 18496
- K042629 — VARELISA SM ANTIBODIES, MODEL 18296
- K041173 — CELIKEY IGG ITG IGG ANTIBODIES, MODEL 17996
- K041357 — VARELISA GLIADIN IGG ANTIBODIES
- K041174 — CELIKEY TTG (HUMAN, RECOMBINANT) IGA ANTIBODIES MODEL #18148/18196
- K041354 — VARELISA GLIADIN IGA ANTIBODIES MODEL #19848/19896
- K041040 — VARELISA MPO ANCA, MODEL 17648/17696
Data sourced from openFDA. This site is unofficial and independent of the FDA.