510(k) Report

FDA applicant

Zeller Power Products (Battery Beast, LLC)

Las Vegas, NV1 decision2014–20140 recalls

FDA records 1 decision for Zeller Power Products (Battery Beast, LLC) (Las Vegas, NV) in 2014: 1 510(k) clearance. All are in product code MKJ (Automated External Defibrillators (Non-Wearable)). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Zeller Power Products (Battery Beast, LLC)’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2014: 1
2014high 1 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Zeller Power Products (Battery Beast, LLC) by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Zeller Power Products (Battery Beast…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • MKJAutomated External Defibrillators (Non-Wearable)1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K141231ZP9141, ZP9146Y, ZP9146W Non-Rechargeable BatteryZeller Power Products (Battery Beast, LLC) · 2014

The one decision as Zeller Power Products (Battery Beast, LLC) →