# K955270: Tape & Bandage, Adhesive

- Pathway: 510(k) (Traditional)
- Applicant: Robert R. Stevens
- Decided: Aug 8, 1996 after 267 days
- Product code: DXC (Clamp, Vascular)
- Device class: 2
- Regulation: 21 CFR 870.4450
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The summary cites one number, which could not be confirmed as its predicate (listed below).

## Cited in the summary but kept off the family tree
- K951973: Cutaneous Compression Device for Hemodialysis. Not in FDA’s 510(k), De Novo or PMA lists as we hold them (a misreading, a typo, or a number FDA does not list), so it is kept off the family tree Summary page 1.

## Most influential descendants
- K964041: Cutaneous Compression Device for Use in Hemodialysis (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K955270
Methodology: https://510kreport.com/methodology