# K981949: Numobag

- Pathway: 510(k) (Traditional)
- Applicant: Numotech, Inc.
- Decided: Feb 3, 1999 after 245 days
- Product code: KPJ (Chamber, Oxygen, Topical, Extremity)
- Device class: 2
- Regulation: 21 CFR 878.5650
- 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
For adjunctive therapy of the following conditions: 1. Skin ulcerations due to diabetes, venous stasis, post surgical infections and gangrenous lesions 2. Decubitus ulcers 3. Amputations/infected stumps 4. Skin grafts 5. Burns 6. Frostbite

Source page: https://510kreport.com/device/K981949
Methodology: https://510kreport.com/methodology