# Cathlab Corp.

- Location (FDA's records): Tustin, CA
- FDA decisions: 8 (1988–1991): 8 510(k) clearances
- Product codes: DXE (4), DQO (1), GCA (1), DYG (1), DQT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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
- American Biomed, Inc.: 2 (https://510kreport.com/company/american-biomed)
- Lucas Medical, Inc.: 1 (https://510kreport.com/company/lucas-medical)

## Its most-cited devices
- K881455: Embolectomy Catheter (Modified) (1988), cited by 1
- K905139: Cathlab Silicone Arterial Embolectomy Catheter (1991), cited by 1
- K910917: Cathlab Silicone Biliary Balloon Catheter (1991), cited by 1

## Recent decisions
- K910917: Cathlab Silicone Biliary Balloon Catheter (Aug 2, 1991)
- K910916: Cathlab Silicone Occlusion Balloon Catheter (Jun 24, 1991)
- K905139: Cathlab Silicone Arterial Embolectomy Catheter (Feb 25, 1991)
- K897051: Miller Percutaneous Angiographic/Scopic Irri. Cath (Mar 16, 1990)
- K897184: 3F and 4F Irrigation Embolectomy Catheters (Mar 14, 1990)
- K893435: Silicone Flow-Directed Thermodilution Catheter (Sep 26, 1989)
- K893680: Silicone BI-Lumen Irrigation Embolectomy Cath. (Aug 1, 1989)
- K881455: Embolectomy Catheter (Modified) (Jun 15, 1988)

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