FDA device listing

5674

FDA device listing 1137217536 · R & D BATTERIES, INC.

Key facts

Proprietary names 5674
Owner/operator R & D BATTERIES, INC.
Owner/operator number 9006991
Premarket submissions K944387
Product codes FCO
Device names FCO - Box, Battery, Rechargeable
Device class Class I
Classification regulations (21 CFR) 876.1500
Review panels Gastroenterology & Urology
Registered establishments R & D BATTERIES, INC.
Establishment registrations 2132111
FEI numbers 1000140026
Establishment operations Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 100–999 UDI devices (GUDID) under the same submission
  • 1–9 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