# K964654: Becton Dickinson Blunt Plastic Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
- Decided: Apr 2, 1997 after 133 days
- Product code: FMI (Needle, Hypodermic, Single Lumen)
- Device class: 2
- Regulation: 21 CFR 880.5570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K854547 (1986). 2 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K854547: Monoject Sterile M200 Aluminum/M250 Polypropylene, Sherwood Medical Co. (1986) Summary page 1.
- K931377: Safeline System IV Administration Sets & Component, Mcgaw, Inc. (1994) Summary page 1.
- (no number) Becton Dickinson interLink® Syringe Cannula: named in the summary without a submission number

## Most influential descendants
- K974363: Becton Dickinson Blunt Plastic Cannula (1998), 1 descendant of its own
- K013949: Universal Vial Access Spike with Needleless Connector (2002), 0 descendants of its own

## Indications for use
The B-D® Blunt Plastic Cannula replaces hypodermic needles currently used to access injection sites, as well as, vials designed for penetration with needleless IV access cannula. The B-D® Blunt Plastic Cannula provides access to the fluid path for injection / aspiration of fluids. Use of this device prevents accidental hypodermic needlesticks in this application.

Source page: https://510kreport.com/device/K964654
Methodology: https://510kreport.com/methodology