# Mallinckroot, Inc.

- Location (FDA's records): St Louis, MO
- FDA decisions: 7 (1988–1999): 7 510(k) clearances
- Product codes: DYB (2), LIT (2), EYB (1), BSK (1), DQO (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 4 (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 whose devices it cites most
- Boston Scientific Corp: 3 (https://510kreport.com/company/boston-scientific)
- Guidant Corp.: 1 (https://510kreport.com/company/guidant)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Peripheral Systems Group: 1 (https://510kreport.com/company/peripheral-systems-group)

## Firms that cite its devices most
- Mentor Medical Limited: 1 (https://510kreport.com/company/mentor-medical)
- Venner Medical (Singapore) Pte, Ltd.: 1 (https://510kreport.com/company/venner-medical-singapore)
- Spiritus Technologies, LLC: 1 (https://510kreport.com/company/spiritus-technologies)
- Bolton Medical, Inc.: 1 (https://510kreport.com/company/bolton-medical)

## Its most-cited devices
- K983830: Copperhead 5 FR. Pta Catheter, Finch 4 FR. Pta Catheter (1999), cited by 2
- K885216: Attachable Lanz (Tentative) (1989), cited by 2

## Recent decisions
- K983830: Copperhead 5 FR. Pta Catheter, Finch 4 FR. Pta Catheter (Apr 16, 1999)
- K894445: Modified Softouch Introducer W/Hemo Valve & Side (Oct 2, 1989)
- K885348: A-V (TM) Softouch Uhf Cardiac Pigtail (May 15, 1989)
- K885216: Attachable Lanz (Tentative) (Mar 14, 1989)
- K884159: Softouch Introducer W/Hemostasis Valve & Sideport (Feb 22, 1989)
- K884481: Clear Shot Angioplasty Balloon Inflation Device (Jan 10, 1989)
- K882130: Foley-Temp (TM) (Aug 9, 1988)

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