Omni Intl., Inc.
Omni Intl., Inc. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 1999.
Top product codes for Omni Intl., Inc.
Recent clearances by Omni Intl., Inc.
- K984066 — OMNIGRIP, LATEX SURGICAL GLOVE, POWDER-FREE WITH PROTEIN LABELING CLAIM
- K984064 — OMNIGRIP, LATEX SURGICAL GLOVE, POWDER FREE
- K853255 — OMNIMED I.V. SOLUTION ADMIN. SET
- K851938 — OMNIMED SURGICAL GOWN
- K851654 — OMNIMED CLAMP
- K851734 — OMNIMED SUPERIOR TRANSDUCER PROTECTOR
- K850706 — F-SERIES IMPLANT
- K850112 — OMNIMED IV SOLUTION ADMINISTRATION SET
- K850066 — OMNIMED NASAL OXYGEN CANNULA
- K831147 — OMNIPROBE ELECTRICAL NERVE STIMULATOR
- K821523 — OMNI TENS
- K813604 — OMNI STIM II
Data sourced from openFDA. This site is unofficial and independent of the FDA.