# Catheter Research, Inc.

- Location (FDA's records): Indianapolis, IN
- FDA decisions: 8 (1994–2013): 8 510(k) clearances
- Product codes: LKF (4), BZT (1), BZA (1), MQF (1), CCK (1)
- Predicates its devices cite: 6 (2 its own); citations of its devices by later devices: 8 (2 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Femasys, Inc.: 1 (https://510kreport.com/company/femasys)
- Ackrad Laboratories: 1 (https://510kreport.com/company/ackrad-laboratories)
- Thomas Medical, Inc.: 1 (https://510kreport.com/company/thomas-medical)
- Fertiligent, Ltd.: 1 (https://510kreport.com/company/fertiligent)

## Firms that cite its devices most
- Cook, Inc.: 2 (https://510kreport.com/company/cook)
- Vyaire Medical, Inc.: 1 (https://510kreport.com/company/vyaire-medical)
- Fertiligent, Ltd.: 1 (https://510kreport.com/company/fertiligent)
- Intersurgical, Inc.: 1 (https://510kreport.com/company/intersurgical)
- Promedic, Inc.: 1 (https://510kreport.com/company/promedic)

## Its most-cited devices
- K946044: Disposable Gas Sampling Lines (1994), cited by 3
- K123258: The Advance Catheter for HSG and Sis (2013), cited by 2
- K032835: H/S Catheter Set (2003), cited by 2
- K020292: Uterine Injector (2002), cited by 1

## Recent decisions
- K123258: The Advance Catheter for HSG and Sis (Jan 31, 2013)
- K120154: Intrauterine Insemination (Iui) Catheter (Mar 21, 2012)
- K032835: H/S Catheter Set (Dec 11, 2003)
- K020292: Uterine Injector (Apr 17, 2002)
- K973839: Disposable Esophageal Stethoscope (Mar 19, 1998)
- K974357: Uterine Manipulator/Injector (Feb 2, 1998)
- K951345: Disposable Airway Connectors for Gas Sampling (Apr 14, 1995)
- K946044: Disposable Gas Sampling Lines (Dec 27, 1994)

Source page: https://510kreport.com/company/catheter-research