# K021033: Stimuplex-Dig-RC Nerve Stimulator

- Pathway: 510(k) (Special)
- Applicant: B.Braun Medical, Inc.
- Decided: Mar 21, 2003 after 357 days
- Product code: BXN (Stimulator, Nerve, Battery-Powered)
- Device class: 2
- Regulation: 21 CFR 868.2775
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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) B. Braun Medical Inc. Stimuplex Nerve Stimulator: named in the summary without a submission number

## Indications for use
The StimuplexO-DIG-RC Nerve Stimulator is intended for use with B. Braun Medical Inc. Stimuple,x and ContiplexB insulated needle sets for use in regional anesthesia and regional pain therapy. Peripheral nerves are stimulated and located via electrical current impulses flowing through an insulated needle.

Source page: https://510kreport.com/device/K021033
Methodology: https://510kreport.com/methodology