# Microsulis Medical Limited

- Location (FDA's records): Denmead Hampshire, GB
- FDA decisions: 3 (2003–2012): 2 510(k) clearances and 1 original PMA approval
- Names in FDA's records: Microsulis Medical Limited (2); Microsulis Medical , Ltd. (1)
- Product codes: NEY (2), MNB (1)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- AngioDynamics, Inc.: 1 (https://510kreport.com/company/angiodynamics)

## Its most-cited devices
- K094021: Acculis ACCU2I Pmta Applicator Model ACCU2I (2010), cited by 1
- K122762: Acculis ACCU21 Pmta Microwave Tissue Ablation Applicator (2012), cited by 1

## Recent decisions
- K122762: Acculis ACCU21 Pmta Microwave Tissue Ablation Applicator (Nov 30, 2012)
- K094021: Acculis ACCU2I Pmta Applicator Model ACCU2I (Aug 6, 2010)
- P020031: Microsulis Microwave Endometrial Ablation (Mea) System (Sep 23, 2003)

Source page: https://510kreport.com/company/microsulis-medical