# K072114: Impulse 6000D/7000DP

- Pathway: 510(k) (Traditional)
- Applicant: Fluke Biomedical
- Decided: Jan 28, 2008 after 180 days
- Product code: DRL (Tester, Defibrillator)
- Device class: 2
- Regulation: 21 CFR 870.5325
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Fluke Biomedical, Impulse 4000: named in the summary without a submission number

## Most influential descendants
- K182905: UniPulse (2018), 0 descendants of its own

## Indications for use
The Impulse 6000D/7000DP is used to determine that defibrillators and transcutaneous pacemakers are performing within their performance specifications through the measurement of energy output.

Source page: https://510kreport.com/device/K072114
Methodology: https://510kreport.com/methodology