# K984564: Ethyl Chloride Dispenser

- Pathway: 510(k) (Traditional)
- Applicant: Dukal Corp.
- Decided: Dec 2, 1999 after 344 days
- Product code: MLY (Vapocoolant Device)
- Device class: U
- 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) Gebauer Fluori-Methane: named in the summary without a submission number

## Indications for use
A vapocoolant intended for topical application in management of myofacial pain, restricted motion, and muscle spasm, and for the control of pain associated with injections, minor surgical procedures and the temporary relief of minor sports injuries.

Source page: https://510kreport.com/device/K984564
Methodology: https://510kreport.com/methodology