# Bypass, Ltd.

- Location (FDA's records): Washington, DC
- FDA decisions: 2 (2001–2002): 2 510(k) clearances
- Product codes: FZP (1), NCA (1)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- United States Surgical, A Division of Tyco Healthc: 2 (https://510kreport.com/company/united-states-surgical-a-division-of-tyco-healthc)
- Cardio Thoracic Systems: 1 (https://510kreport.com/company/cardio-thoracic-systems)

## Firms that cite its devices most
- By-Pass Makafim, Ltd.: 1 (https://510kreport.com/company/by-pass-makafim)

## Its most-cited devices
- K020470: Modification to Corlink Automated Anastomotic Device (2002), cited by 1
- K011589: Corlink Aad (3.5 to 6.0 M M Outer Diameter Vessels),Model 200-064, Corlink Aad (2.0 to 4.0 MM Outer Diameter Vessels), M (2001), cited by 1

## Recent decisions
- K020470: Modification to Corlink Automated Anastomotic Device (Mar 8, 2002)
- K011589: Corlink Aad (3.5 to 6.0 M M Outer Diameter Vessels),Model 200-064, Corlink Aad (2.0 to 4.0 MM Outer Diameter Vessels), M (Dec 26, 2001)

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