# K133632: Perican Ultra

- Pathway: 510(k) (Traditional)
- Applicant: B.Braun Medical, Inc.
- Decided: Jun 27, 2014 after 213 days
- Product code: BSP (Needle, Conduction, Anesthetic (W/Wo Introducer))
- Device class: 2
- Regulation: 21 CFR 868.5150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K840287 (1984). 22 ancestors in all.
1 later device descends from it; 1 cites it directly.
3 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K113059: Contiplex FX, B.Braun Medical, Inc. (2012) Summary page 1.
- K113207: Sono Tap, Tuohy Sono, Pajunk GmbH (2012)

## Most influential descendants
- K150266: Remington Medical Inc. Tuohy Epidural Needles (2015), 0 descendants of its own

## Indications for use
The B. Braun Perican Ultra needle is intended for use in injecting local anesthetics and/or analgesics into a patient to provide regional anesthesia and/or analgesia and/or to facilitate the placement of a catheter.

Source page: https://510kreport.com/device/K133632
Methodology: https://510kreport.com/methodology