FDA device listing

C5 LoFlo Sidestream Module,Carescape CO2 - LoFlo,Cobranded LoFlo CO2 Sampling Cannula,Cobranded LoFlo Sampling Line…

FDA device listing 1948105782 · Philips Medical Systems International BV

Key facts

Proprietary names C5 LoFlo Sidestream Module,Carescape CO2 - LoFlo,Cobranded LoFlo CO2 Sampling Cannula,Cobranded LoFlo Sampling Line Kit,Cobranded LoFlo Sampling Line Kit w/Dehumidification Tubing,LoFlo Airway Adapter Kit ADULT/PEDIATRIC,LoFlo Airway Adapter Kit INFANT/NEONATAL,LoFlo Airway Adapter Kit w/ Dehumidification Tubing Adult/Pediatric,LoFlo Airway Adapter Kit w/Dehumidification Tubing…
Owner/operator Philips Medical Systems International BV
Owner/operator number 1217116
Premarket submissions K053174
Product codes CCK
Device names CCK - Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Device class Class II
Classification regulations (21 CFR) 868.1400
Review panels Anesthesiology
Registered establishments Philips Electronics Ltd, Philips Medical Systems Ltda, Philips North America LLC, RESPIRONICS NOVAMETRIX, LLC
Establishment registrations 1219324, 3000126629, 3014541700, 3016618143
FEI numbers 1219324, 3000126629, 3014541700, 3016618143
Establishment operations Complaint File Establishment, Foreign Exporter, Specification Developer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None UDI devices (GUDID) under the same submission
  • 10–99 Device listings citing the same submission
  • Yes 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

Browse all FDA device listings