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ZP9141, ZP9146Y, ZP9146W Non-Rechargeable Battery

by Zeller Power Products (Battery Beast, LLC)

510(k) K141231

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK141231 Date25 Nov 2014ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
MKJ
Device Class
Class III
Regulation
21 CFR Part 870.5310
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 20 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

This device is a non-rechargeable battery designed for use in automated external defibrillators (non-wearable). It serves as a disposable power source, providing the necessary electrical energy for defibrillation and monitoring functions in cardiac arrest emergencies. The battery is engineered to replace existing battery packs in compatible defibrillator models, ensuring uninterrupted operation during critical interventions.

The ZP9141, ZP9146Y, and ZP9146W batteries are supplied as single-use, non-rechargeable units with a shelf life of five years from the date of manufacture. They are intended for use in specific defibrillator models, including Cardiac Science PowerHeart® Non-G3 and Survivalink Non-G3 systems. Regulated under FDA 510(k) clearance (K141231) and classified under regulation 870.5310, these batteries are not intended for MRI environments and must be handled and stored according to manufacturer guidelines to maintain functionality and safety.

Questions

AI-generated answers, 20 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • Are these batteries compatible with any defibrillator model, or only specific ones? If so, which ones?

    These batteries (ZP9141, ZP9146Y, and ZP9146W) are designed exclusively for use in Cardiac Science PowerHeart® Non-G3 and Survivalink Non-G3 automated external defibrillator systems. They replace existing battery packs in these specific models to ensure proper functionality during cardiac arrest emergencies.

  • How long can these batteries be stored before they expire, and what happens if they’re used past their shelf life?

    The batteries have a five-year shelf life from the date of manufacture. Using them beyond this period may compromise performance, as the manufacturer’s guidelines emphasize proper storage to maintain functionality and safety. Always check the expiration date before use.

  • Can these batteries be recharged, or are they strictly single-use?

    These are non-rechargeable, single-use batteries. They are engineered as disposable power sources for defibrillators, ensuring reliable operation during emergencies without the risk of recharging failures or degradation.

  • Are these batteries safe to use near MRI machines, or should they be kept away?

    The manufacturer explicitly states these batteries are not intended for MRI environments. They should be stored and used away from MRI equipment to avoid potential interference or safety risks.

  • What regulatory pathway was followed for these batteries, and which committee reviewed them?

    These batteries were cleared through the FDA’s 510(k) process (K141231), classified under regulation 870.5310, and reviewed by the Cardiovascular (CV) Advisory Committee. The clearance type is traditional, and they are classified as Class III medical devices for automated external defibrillators.