Disease Detection International, Inc.
FDA 510(k) medical device clearances.
Top product codes for Disease Detection International, Inc.
Recent clearances by Disease Detection International, Inc.
- K943252 — PRO-STEP LH OVULATION PREDICTION TEST
- K925303 — PRO-STEP PT HCG
- K925125 — PRO-STEP HCG
- K911826 — IMMUNOCARD HCG ONE STEP (I-S) TEST KIT
- K902571 — MODIFICATION OF SEROCARD RUBELLA IGG TEST
- K903070 — SEROCARD HSV IGG ANTIBODY TEST KIT
- K895912 — IMMUNOCARD HCG II-S TEST KIT
- K896109 — IMMUNOCARD STREP A TEST
- K884246 — MODIFIED DDI SEROCARD HERPES IGG TEST KIT
- K884247 — MODIFIED DDI SEROCARD RUBELLA IGG TEST KIT
- K884248 — MODIFIED DDI SEROCARD CMV IGG TEST KIT
- K884249 — MODIFIED DDI SEROCARD TOXOPLASMA IGG TEST KIT
- K884047 — FLUOROSLIDE PNEUMOCYSTIS CARINII (IFA) ASSAY
- K883430 — PREGNA-CARD(TM) A VISUAL HOME PREGNANCY TEST
- K881709 — IMMUNOCARD(TM) HCG II TEST KIT
- K875366 — THE DDI SERODOT HERPES IGG TEST KIT
- K875361 — SERODOT CMV (CYTOMEGALOVIRUS) IGG TEST KIT
- K875363 — SERODOT TOXOPLASMA IGG TEST KIT
- K880410 — HUMAN CHORIONIC GONADOTROPIN VISUAL TEST KIT
- K875368 — THE DDI SERODOT RUBELLA IGG TEST KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.