# K930548: DPD Defibrillator

- Pathway: 510(k) (Traditional)
- Applicant: Medical Research Laboratories, Inc.
- Decided: Jun 25, 1993 after 142 days
- Product code: LDD (Dc-Defibrillator, Low-Energy, (Including Paddles))
- Device class: 2
- Regulation: 21 CFR 870.5300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K032051: Battery Pack, Rechargeable, Models MLA0051, MLA90479, MNC5169L/P, MNC1000EKG, MNC14649P (2004), 1 descendant of its own
- K071164: Life+Cel Battery (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K930548
Methodology: https://510kreport.com/methodology