Litton Bionetics
Litton Bionetics holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1984.
Top product codes for Litton Bionetics
Recent clearances by Litton Bionetics
- K840417 — EBNA ACIF KIT
- K834443 — ROTAVIRUS BIO-ENZABEAD SCREEN KIT
- K831343 — CMV RQ BIO-ENZABEAD KIT
- K822985 — EBV-M KIT
- K821804 — RUBELLA RQ BIO-ENZABEAD KIT
- K801720 — TOXO BIO-BEAD TITRATION KIT
- K801721 — HSV BIO-BEAD TITRATION KIT
- K801722 — CMV BIO-BEAD TITRATION KIT
- K800789 — RUBELLA BIO-BEAD TITRATION KIT
- K791610 — RUBELLA BIO-BEAD SCREEN KIT
- K791611 — TOXO BIO-BEAD SCREEN KIT
- K791612 — CMV BIO-BEAD SCREEN KIT
- K791614 — HSV BIO-BEAD SCREEN KIT
- K791618 — TORCH BIO-BEAD SCREEN KIT
- K780925 — EB-VCA, TEST, ANTIBODY, FLUORESCENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.