# K973693: Aqua Patch

- Pathway: 510(k) (Traditional)
- Applicant: Pci Technology
- Decided: Dec 18, 1997 after 83 days
- Product code: MGQ (Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic)
- Device class: U
- 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. The FDA summary names no predicate by number.

## Indications for use
Dermal ulcers, superficial wounds, 1* and 2™ degree burns, donor sites, skin tears, radiation reactions (burns), protection around tube sites.

Source page: https://510kreport.com/device/K973693
Methodology: https://510kreport.com/methodology