# Angiosystems, Inc.

- Location (FDA's records): Great Neck, NY
- FDA decisions: 14 (1984–1991): 14 510(k) clearances
- Product codes: KKX (3), EKS (1), HMT (1), CBT (1), NAD (1), LRO (1), LRP (1), DRE (1), FOZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

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

## Its most-cited devices
- K905464: Medical Procedure Kits/Arterial Blood Sampling (1991), cited by 1

## Recent decisions
- K905464: Medical Procedure Kits/Arterial Blood Sampling (May 31, 1991)
- K905459: Surgical Procedure Tray/Laparoscopy Cholecystectom (Apr 5, 1991)
- K905461: Procedure Kit/Routine Dental Procedures (Mar 5, 1991)
- K905465: Sterile Dispos Surgical Drape/C-Section Drape (Feb 11, 1991)
- K905466: Sterile Disposable Surgical Drape/Abdominal Drape (Feb 11, 1991)
- K905460: Sterile Disposable Drape/Ophthalmic Surgery (Feb 6, 1991)
- K905462: Procedure Tray/for Various Ophthalmic Procedures (Feb 6, 1991)
- K905463: General Medical Procedure Kit/Skin Preparation (Jan 22, 1991)

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