FDA device listing

Neilmed6807 (NT) - NeilMed NasaMist Extra Strength (Hypertonic) Saline Spray,Neilmed6807 (NT) - NeilMed…

FDA device listing 1165788123 · STERIS Corporation

Key facts

Proprietary names Neilmed6807 (NT) - NeilMed NasaMist Extra Strength (Hypertonic) Saline Spray,Neilmed6807 (NT) - NeilMed SinuHale,Neilmed6807 (NT,SN*) - NasaMist - Isotonic,Neilmed6807 (NT,SN*) - Ultra Gentle Spray,Neilmed6807 (NT,SN*) - Walgreen Nasal Mist,Neilmed6807 (NT) - Walgreens Nasal Mist
Owner/operator STERIS Corporation
Owner/operator number 1527821
Product codes KCO
Device names KCO - Nasal Spray, Ent Delivery
Device class Class I
Classification regulations (21 CFR) 874.5220
Review panels Ear, Nose, & Throat
Registered establishments Isomedix Operations, Inc, Isomedix Operations, Inc., ISOMEDIX OPERATIONS INC, ISOMEDIX OPERATIONS INC.
Establishment registrations 1424263, 1450662, 1526711, 1720929, 2032098
FEI numbers 1450662, 1526711, 1720929, 3003015552, 3003058448
Establishment operations Contract Sterilizer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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