# Burron Medical, Inc.

- Location (FDA's records): Bethlehem, PA
- FDA decisions: 9 (1988–1991): 9 510(k) clearances
- Product codes: FRN (3), DRS (1), FOZ (1), DQX (1), FMF (1), LJT (1), CAZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 10 (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
- I-Flow Corp.: 6 (https://510kreport.com/company/i-flow)
- Advanced Infusion, Inc.: 1 (https://510kreport.com/company/advanced-infusion)
- Sgarlato Laboratories, Inc.: 1 (https://510kreport.com/company/sgarlato-laboratories)
- B.Braun Medical, Inc.: 1 (https://510kreport.com/company/b-braun-medical)
- Aesculap, Inc.: 1 (https://510kreport.com/company/aesculap)

## Its most-cited devices
- K896422: Burron Ambulatory Drug Delivery System (1990), cited by 8
- K902401: Celsite (TM) Implantable Drug Delivery System (1991), cited by 2

## Recent decisions
- K902401: Celsite (TM) Implantable Drug Delivery System (Oct 8, 1991)
- K896422: Burron Ambulatory Drug Delivery System (May 9, 1990)
- K884235: Combitrans Disposable Pressure Transducer Kit (Mar 6, 1990)
- K895191: Anti-Thrombogenic Coating for Catheters (Nov 24, 1989)
- K895192: Spinocan (R) Continuous Spinal Tray (Sep 18, 1989)
- K884183: Burron Teflon-Coated Guidewire (Aug 3, 1989)
- K882107: Perfusor Secura Syringe Pump (Aug 11, 1988)
- K882106: Perfusor M Syringe Pump (Aug 11, 1988)

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