# Micor, Inc.

- Location (FDA's records): Allison Park, PA
- FDA decisions: 8 (1986–2003): 8 510(k) clearances
- Product codes: BSO (2), DQY (2), FRN (2), DQO (1), CAZ (1)
- Predicates its devices cite: 6 (3 its own); citations of its devices by later devices: 8 (3 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
- Epimed International, Inc.: 1 (https://510kreport.com/company/epimed-international)
- Preferred Medical Products: 1 (https://510kreport.com/company/preferred-medical-products)
- Breg, Inc.: 1 (https://510kreport.com/company/breg)

## Firms that cite its devices most
- Mckinley Medical, LLC: 2 (https://510kreport.com/company/mckinley-medical)
- American Medical Technologies, Inc.: 1 (https://510kreport.com/company/american-medical-technologies)
- B.Braun Medical, Inc.: 1 (https://510kreport.com/company/b-braun-medical)
- Busse Hospital Disposables, Inc.: 1 (https://510kreport.com/company/busse-hospital-disposables)

## Its most-cited devices
- K991879: Spring-Wound Epidural Catheter (1999), cited by 3
- K001717: Micor Conduction Catheter (2000), cited by 2
- K003966: Wundcath Conduction Catheter (2001), cited by 2
- K031600: Conduction Catheter (2003), cited by 1

## Recent decisions
- K031600: Conduction Catheter (Aug 13, 2003)
- K003966: Wundcath Conduction Catheter (Jul 17, 2001)
- K001717: Micor Conduction Catheter (Sep 20, 2000)
- K001940: Micor Anesthesia Conduction Kit (Aug 11, 2000)
- K991879: Spring-Wound Epidural Catheter (Oct 28, 1999)
- K861008: Percutaneous Catheters (Apr 29, 1986)
- K860339: Percutaneous Catheters (Mar 31, 1986)
- K854018: Angiography Catheters (Jan 16, 1986)

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