FDA device listing

CDC100,CDC100B,CDC200,CDC200S,CDC300S,CDC500,CDC500S, CDC500B,CNB69012, CNB69015, CNB69016, CNB69017, CNB69018…

FDA device listing 1794168954 · Shenzhen Fitconn Technology Co., Ltd

Key facts

Proprietary names CDC100,CDC100B,CDC200,CDC200S,CDC300S,CDC500,CDC500S, CDC500B,CNB69012, CNB69015, CNB69016, CNB69017, CNB69018, CNB69020, CNB69021, CNB69022, CNB69025, CNB69021S, CNB69025S, CNB69026,CNB69028, CNB69029, CNB69029S, CNB69031, CNB69031S,COMPRESSOR NEBULIZER, Models: CNB69006,CNB69007,CNB69008,CNB69009,CNB69010, CNB69011
Owner/operator Shenzhen Fitconn Technology Co., Ltd
Owner/operator number 10059755
Product codes BTI
Device names BTI - Compressor, Air, Portable
Device class Class II
Classification regulations (21 CFR) 868.6250
Review panels Anesthesiology
Registered establishments SHENZHEN FITCONN TECHNOLOGY CO., LTD
Establishment registrations 3015219192
FEI numbers 3015219192
Establishment operations Manufacturer
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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