# K902889: A1-a,A1-B,A1-Abp,A1-MBP,A1-Z,A6-a,A6-B,Peh Pace.

- Pathway: 510(k) (Traditional)
- Applicant: Biotronik, GmbH & Co.
- Decided: Aug 23, 1990 after 52 days
- Product code: DTD (Pacemaker Lead Adaptor)
- Device class: 2
- Regulation: 21 CFR 870.3620
- 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. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K970388: A1-a,Abp,B,MBP, Lead Connectors; Peh Adapter Sleeve (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K902889
Methodology: https://510kreport.com/methodology