# Keller Medical Specialties Products, Inc.

- Location (FDA's records): Antioch, IL
- FDA decisions: 6 (1990–1999): 6 510(k) clearances
- Product codes: DQA (2), DSJ (1), DXN (1), DRT (1), DRO (1)
- Predicates its devices cite: 4 (3 its own); citations of its devices by later devices: 3 (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
- Criticare Systems, Inc.: 1 (https://510kreport.com/company/criticare-systems)

## Its most-cited devices
- K982331: Keller Pulse Oximeter, Model 850+ (1998), cited by 1
- K910262: Keller Vital Signs Monitor - KMS-890 (1991), cited by 1
- K895987: Keller Pulse Oximeter - KMS 850 (1990), cited by 1

## Recent decisions
- K990648: Keller Vital Signs Monitor, KMS 890+ (Aug 10, 1999)
- K982331: Keller Pulse Oximeter, Model 850+ (Sep 11, 1998)
- K914576: Keller Cardiac Monitor Medil KMS870 (Dec 30, 1991)
- K910262: Keller Vital Signs Monitor - KMS-890 (Apr 1, 1991)
- K903437: Dispos  Access  External Cardiac Pacemaker (Nov 16, 1990)
- K895987: Keller Pulse Oximeter - KMS 850 (Feb 22, 1990)

Source page: https://510kreport.com/company/keller-medical-specialties-products