# K012917: Dynarex Umbilical Cord Lamp, Models 6833 and 6833-B

- Pathway: 510(k) (Traditional)
- Applicant: Dynarex Corp.
- Decided: Nov 28, 2001 after 90 days
- Product code: HFW (Clamp, Umbilical)
- Device class: 2
- Regulation: 21 CFR 884.4530
- 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 no predicate by number.

## Indications for use
The Dynarex Umbilical Cord Clamp is a device used to compress the umbilical cord. Federal (USA) law restricts this device to sale by or on the order of a physician.

Source page: https://510kreport.com/device/K012917
Methodology: https://510kreport.com/methodology