# K895920: Vitapatch Pin Protection Device for Percutaneous

- Pathway: 510(k) (Traditional)
- Applicant: Vitaphore Corp.
- Decided: Jun 6, 1991 after 603 days
- Product code: KGX (Tape And Bandage, Adhesive)
- Device class: 1
- Regulation: 21 CFR 880.5240
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
32 later devices descend from it; 1 cites it directly.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K003229: Biopatch Antimicrobial Dressing (2001), 31 descendants of its own
- K063458: 3M Tegaderm CHG Dressing (2007), 16 descendants of its own
- K080779: Irrisept Wound Cleansing System (2009), 9 descendants of its own
- K202222: Irrisept Wound Debridement and Cleansing System (2020), 7 descendants of its own
- K080620: Modification to 3M Tegaderm CHG Dressing (2008), 7 descendants of its own

Source page: https://510kreport.com/device/K895920
Methodology: https://510kreport.com/methodology