# K883930: Seamed Model 3300 Dual Chamber Pacing System Analy

- Pathway: 510(k) (Traditional)
- Applicant: Seamed Corp.
- Decided: Nov 9, 1988 after 55 days
- Product code: DTE (Pulse-Generator, Pacemaker, External)
- Device class: 2
- Regulation: 21 CFR 870.3600
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K964190: Era 300 Dual Chamber Pacing System Analyzer (1997), 9 descendants of its own
- K022360: Era 3000; PA-2 IS-1 Adapter; EK-4-N Pacemaker Test Cable; Era 3000 Charger; Era 3000 Battery (Type 2); NK-11 Power Supp. (2003), 4 descendants of its own
- K083674: PK-141 Patient Cable (2009), 1 descendant of its own
- K033613: Modification to Era 300 Dual Chamber Pacing System Analyzer (2003), 1 descendant of its own
- K170815: PSA Cable (2017), 0 descendants of its own

Source page: https://510kreport.com/device/K883930
Methodology: https://510kreport.com/methodology