# K242937: Dream Medi Sterile Surgical Gown (SurgicalGownUL)

- Pathway: 510(k) (Traditional)
- Applicant: Dae Myung Chemical Co., Ltd. (Vietnam)
- Decided: May 5, 2025 after 222 days
- Product code: FYA (Gown, Surgical)
- Device class: 2
- Regulation: 21 CFR 878.4040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K020593 (2002). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K222999: Surgical Gown, Hubei Woozon Healthcare Co., Ltd. (2023) Summary page 5.

## Indications for use
The Dream Medi Sterile Surgical Gowns are intended to be worn by operating room personnel during surgical procedures to protect the surgical patient and operating room personnel from the transfer of microorganisms, body fluids and particulate matter. In addition, this surgical gown meets the requirements of AAMI Level 3 barrier protection for a surgical gown per ANSI/AAMI PB70 Liquid barrier performance and classification of protective apparel and drapes intended for use in health care facilities (AAMI PB70). This is a single use, disposable device, provided sterile.

Source page: https://510kreport.com/device/K242937
Methodology: https://510kreport.com/methodology