# Vasca, Inc.

- Location (FDA's records): Tewksburt, MA
- FDA decisions: 2 (2000–2003): 2 510(k) clearances
- Product codes: MSD (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medical Components, Inc.: 1 (https://510kreport.com/company/medical-components)
- Davol, Inc.: 1 (https://510kreport.com/company/davol)

## Recent decisions
- K023023: Lifesite Hemodialysis Access System, Cannula Exchange Kit, Insertion Kit, Access Cannila (Dec 4, 2003)
- K001633: Lifesite Hemodialysis Access System/Cannula Exchange, Model LHAS14120 & LHCEK0000 (Aug 24, 2000)

Source page: https://510kreport.com/company/vasca