Disease Detection International, Inc.
Disease Detection International, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1994.
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.