# K120339: Procoll

- Pathway: 510(k) (Traditional)
- Applicant: Innocoll Pharmaceuticals
- Decided: Jun 21, 2012 after 139 days
- Product code: KGN (Wound Dressing With Animal-Derived Material(S))
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K910944 (1991). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K092805: Collagen Sponge, Innocoll Pharmaceuticals (2010) Summary page 1.

## Indications for use
Procoll may be used for the management of full and partial thickness wounds including: Diabetic ulcers Venous ulcers Pressure ulcers Ulcers caused by mixed vascular etiologies Abrasions Traumatic wounds 1 st and 2 nd degree burns Dehisced surgical wounds Exuding wounds

Source page: https://510kreport.com/device/K120339
Methodology: https://510kreport.com/methodology