# Devcom, Inc.

- Location (FDA's records): Paoli, PA
- FDA decisions: 6 (1985–1990): 6 510(k) clearances
- Product codes: KPR (1), JDL (1), DXQ (1), IKK (1), DPS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K902378: Cardiothoracic Ruler (Jun 14, 1990)
- K874233: Blood Pressure Sleeve W/Tubing (Mar 22, 1988)
- K863313: Grip Strength Device (GSD) (Sep 9, 1986)
- K861264: Joint Measurement Indicator (Apr 15, 1986)
- K861043: Spinal Excursion Meter (Mar 28, 1986)
- K850021: Electrocardiograph-Ecg Caliper (Feb 8, 1985)

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