R&D Batteries, Inc. 6685

• FDA 510(k) K935377 decided 5 Dec 1994 Active
• FDA GUDID UDI-DI 00810149098093 listed 15 Oct 2025 Listed

1. 5 Dec 1994 Cleared FDA 510(k) K935377
2. 15 Oct 2025 Listed FDA GUDID 00810149098093

Trade name

R&D Batteries, Inc.

Generic name

Portable/mobile rechargeable battery pack

Model / reference

6685

Primary DI / UDI-DI

00810149098093

510(k) Number

K935377 ↗

FDA product code

HGM

GMDN term

Portable/mobile rechargeable battery pack

Device class

Class II

Regulation number

884.2740

GUDID distribution status

In Commercial Distribution

Other devices filed under FDA product code HGM (System, monitoring, perinatal).

• Model 2106 Feta Sonde Fetal Monitor by Roche Medical Electronics, Inc.
• Baby Dopplex 3000 Mk 2 (BD3000) by Huntleigh Healthcare, Ltd.
• Model U-1000 With Gestational Age Calculation by FUKUDA DENSHI USA, INC.
• Philips Avalon Fetal Monitors FM20 and FM30 by Philips Medizinsysteme Boeblingen GmbH, Cardiac AN
• Sonicaid Model Meridian 800 by Oxford Medilog, Inc.
• PHILIPS AVALON FETAL / MATERNAL MONITORS FM20, FM30, FM40 AND FM50 by Philips Medizin Systeme Böblingen GmbH
• NOVII+ POD by Datex-Ohmeda Inc.
• Model 855 Enhanced Performance Remote Terminal by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.
• Philips Avalon CTS Cordless Fetal Transducer System, Models M2720A, M2725A, M2726A, M2727A by Philips Medical Systems
• Model M1310A Series 50T Fetal Telemetry System by Hewlett-Packard Co.

• R&D Batteries, Inc. 6580-A

  Class II

  FDA 510(k) K935377 Active Cleared 5 Dec 1994 GUDID on market

• R&D Batteries, Inc. 6581-A

  Class I

  GUDID on market

• R&D Batteries, Inc. 6583-A

  Class I

  GUDID on market

• R&D Batteries, Inc. 6584-A

  Class II

  FDA 510(k) K935377 Active Cleared 5 Dec 1994 GUDID on market

See all devices from R & D Batteries, Inc. →