# Circulatory Technology, Inc.

- Location (FDA's records): Oyster Bay, NY
- FDA decisions: 9 (1994–2014): 9 510(k) clearances
- Product codes: DTN (4), DWF (2), FIB (1), KZD (1), MNJ (1)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 4 (2 its own)
- Recalls linked to its devices: 7 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Electromedics, Inc.: 1 (https://510kreport.com/company/electromedics)

## Firms that cite its devices most
- Innovx Medical, Inc.: 1 (https://510kreport.com/company/innovx-medical)
- Gish Biomedical, Inc.: 1 (https://510kreport.com/company/gish-biomedical)

## Its most-cited devices
- K964337: Better-Bladder (BB) (1997), cited by 1
- K001822: The V-Bag (2000), cited by 1
- K964205: Better-Tubing (1998), cited by 1
- K981284: Better-Bladder (BB) (1998), cited by 1

## Recent decisions
- K140321: Initary Better Bladder-Pediatric (Apr 17, 2014)
- K012942: The V Bag, Catalog Number VB1800; Vac-Box for Vacuum Assisted Venous Drainage, Catalog Number VACBOX1500 (Nov 5, 2001)
- K001822: The V-Bag (Jul 7, 2000)
- K981284: Better-Bladder (BB) (Aug 12, 1998)
- K964205: Better-Tubing (Apr 8, 1998)
- K964337: Better-Bladder (BB) (May 23, 1997)
- K961594: Better-Venter (Sep 5, 1996)
- K941492: Pressure Relief Valve (Oct 26, 1994)

Source page: https://510kreport.com/company/circulatory-technology