# K973865: Birtcher UV Lamp

- Pathway: 510(k) (Traditional)
- Applicant: Medfaxx, Inc.
- Decided: Feb 26, 1999 after 508 days
- Product code: MXG (Lamp, Uvc, (For Treating Skin And Wounds))
- Device class: 2
- Regulation: 21 CFR 878.4630
- 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The above device can be used for [illegible] of [illegible] disorders. The product is also [illegible] in the treatment of [illegible] open wounds, [illegible] for protection of [illegible] and [illegible] tissues in the wound [illegible].

Source page: https://510kreport.com/device/K973865
Methodology: https://510kreport.com/methodology