Cleared Traditional

K935111 - UNIPOWERR RECHARGEABLE BATTERY PACK

K935111 is the FDA 510(k) clearance for UNIPOWERR RECHARGEABLE BATTERY PACK by Unipower Corp.. It is a Class 2 Cardiovascular device (product code LDD) cleared through the Traditional 510(k) pathway after a 154-day FDA review.

K935111 · Unipower Corp. · Cardiovascular device
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Mar 1994
Decision
154d
Days
Class 2
Risk

K935111 is an FDA 510(k) clearance for the UNIPOWERR RECHARGEABLE BATTERY PACK. Classified as Dc-defibrillator, Low-energy, (including Paddles) (product code LDD), Class II - Special Controls.

Submitted by Unipower Corp. (Minneapolis, US). The FDA issued a Cleared decision on March 28, 1994 after a review of 154 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.5300 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Unipower Corp. devices

Submission Details

510(k) Number K935111 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 25, 1993
Decision Date March 28, 1994
Days to Decision 154 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
29d slower than avg
Panel avg: 125d · This submission: 154d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code LDD Dc-defibrillator, Low-energy, (including Paddles)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.5300
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - LDD Dc-defibrillator, Low-energy, (including Paddles)

All 45
Devices cleared under the same product code (LDD) and FDA review panel - the closest regulatory comparables to K935111.
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