# K083347: Impulse 7010 Defibrillator Selectable Loads

- Pathway: 510(k) (Traditional)
- Applicant: Fluke Biomedical
- Decided: Dec 24, 2008 after 41 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) Phase 3 Variable Load Module (VLM): named in the summary without a submission number

## Most influential descendants
- K153210: Defibrillator Analyzer Variable Load (2015), 0 descendants of its own

## Indications for use
The impulse 7010 is used to determine that a defibrillator is performing within its operating specifications by providing multiple loads of 25, 50, 75, 100, 125, 150, 175 and 200 Ohms. The Impulse 7010 is used in conjunction with the Impulse 7000DP Defibrillator Analyzer.

Source page: https://510kreport.com/device/K083347
Methodology: https://510kreport.com/methodology