# Pharmaseal Div., Baxter Healthcare Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 24 (1976–1979): 24 510(k) clearances
- Product codes: KNX (3), FMF (3), KOD (2), JBQ (2), CAH (2), FMA (1), HIO (1), FMI (1), OJU (1), KDD (1), KRA (1), DQO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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
- Merit Medical Systems, Inc.: 1 (https://510kreport.com/company/merit-medical-systems)
- Argon Medical Devices, Inc.: 1 (https://510kreport.com/company/argon-medical-devices)

## Its most-cited devices
- K792141: Continuous Flush Device (1979), cited by 2

## Recent decisions
- K792369: Hyperalimentation Dressing Tray (Dec 10, 1979)
- K792141: Continuous Flush Device (Dec 5, 1979)
- K792019: Phadecode XA Inhibitor Assay (Nov 5, 1979)
- K791773: Ventilator Tube with Filter (Oct 22, 1979)
- K791156: Amipaque Myelogram Tray (Jul 30, 1979)
- K790896: Two-Way Anesthesia Filter (Jun 5, 1979)
- K790409: Low Dead Space Insulin Syringe (Apr 24, 1979)
- K782069: Tray, Auxillary Block (Jan 4, 1979)

Source page: https://510kreport.com/company/pharmaseal-div-baxter-healthcare