# Dryden Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 21 (1976–1988): 21 510(k) clearances
- Product codes: CAI (4), BZO (3), CAH (3), BTM (1), BSJ (1), GAX (1), BTQ (1), BTC (1), BSY (1), BZE (1), CAE (1), CCK (1)
- Predicates its devices cite: 0 (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 that cite its devices most
- Hudson Respiratory Care, Inc.: 2 (https://510kreport.com/company/hudson-respiratory-care)
- Promedic, Inc.: 1 (https://510kreport.com/company/promedic)
- Marquest Medical Products, Inc.: 1 (https://510kreport.com/company/marquest-medical-products)

## Its most-cited devices
- K792097: Dryden Bacteria Filter (1979), cited by 1
- K760371: Vent-O2-Cath (1976), cited by 1
- K841722: Mass Spectrometer Interface (1984), cited by 1
- K833066: Dryden Mini Bacteria Filter (1983), cited by 1

## Recent decisions
- K880923: Patient Ventilator Isolator (Sep 6, 1988)
- K880769: Breathing Circuit W/Heated Wire (Aug 24, 1988)
- K882285: Nonrebreathing Circuit (Aug 16, 1988)
- K873928: Universal Tourniquet (Oct 23, 1987)
- K873927: Reuseable Breathing Tubes (Oct 20, 1987)
- K870859: Bag-Tail Bleed Valve (Aug 3, 1987)
- K871386: Breathing Circuit (May 29, 1987)
- K870858: Badgwell Sampling Catheter (May 14, 1987)

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