# Parke-Davis Co.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 47 (1976–1986): 47 510(k) clearances
- Product codes: FOZ (14), DYG (3), BSO (3), FRC (2), KGO (2), KRA (2), DQO (2), KKX (1), EFQ (1), LJS (1), IPG (1), DYB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Spsmedical Supply Corp.: 1 (https://510kreport.com/company/spsmedical-supply)
- 3M Company: 1 (https://510kreport.com/company/3m)
- Becton Dickinson Infusion Therapy Systems, Inc.: 1 (https://510kreport.com/company/becton-dickinson-infusion-therapy-systems)

## Its most-cited devices
- K841168: Sterilization Process Indicator (1984), cited by 2
- K843033: Deseret Intravascular Catheter (1984), cited by 1

## Recent decisions
- K861725: Intracath Intravenous Catheter Placement Unit (Dec 4, 1986)
- K862119: Deseret Flo-Thru Injectate Temperature Sensor (Aug 29, 1986)
- K855120: Ati Disposable Biological Test Pack (Jun 18, 1986)
- K860570: Angio-Flo Continuous Arterial Cath Flush Device (Mar 31, 1986)
- K860290: Viapic Central Line Catheter (Mar 18, 1986)
- K852192: Disposable Steam Biological Test Pack (Nov 1, 1985)
- K841967: Deseret Thermodilution Cardiac Output (Aug 19, 1985)
- K851327: Deseret Arterial Catheter (Jun 14, 1985)

Source page: https://510kreport.com/company/parke-davis