# K964029: Emergency Relief Kit System

- Pathway: 510(k) (Traditional)
- Applicant: Baxter Healthcare Corp
- Decided: Mar 17, 1997 after 161 days
- Product code: LRR (First Aid Kit With Drug)
- Device class: N
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K952786 (1995). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K952786: Triflex Sterile Synthetic Examination Gloves, Baxter Healthcare Corp (1995) Summary page 1.
- (no number) Gauze Dressing: named in the summary without a submission number
- (no number) Oval Eye Pad: named in the summary without a submission number
- (no number) Adhesive Tape: named in the summary without a submission number
- (no number) Scissors: named in the summary without a submission number
- (no number) Sterile Saline for Eye Irrigation: named in the summary without a submission number
- (no number) Metal Extremity Splint: named in the summary without a submission number
- (no number) Cold Pack: named in the summary without a submission number
- (no number) Bandage Strips: named in the summary without a submission number
- (no number) Topical Antiseptic Ointment: named in the summary without a submission number
- (no number) Alcohol Swab: named in the summary without a submission number

## Indications for use
The Baxter Emergency Relief ™ System consists of color-coded mini first aid kits. Each kit is intended to be used as a basic first aid treatment for various emergency situations, while seeking further professional medical assistance.

Source page: https://510kreport.com/device/K964029
Methodology: https://510kreport.com/methodology