# Core-M, Inc.

- Location (FDA's records): Allston, MA
- FDA decisions: 4 (1989–1996): 4 510(k) clearances
- Names in FDA's records: Core-M, Inc. (3); Core-M, L.P. (1)
- Product codes: CAP (2), CCL (1), CBK (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Draeger Medical, Inc.: 1 (https://510kreport.com/company/draeger-medical)

## Its most-cited devices
- K960861: Omicron Monitor, Delta Monitor (1996), cited by 1

## Recent decisions
- K960861: Omicron Monitor, Delta Monitor (Aug 19, 1996)
- K944120: FI02 Sensing Module (May 10, 1995)
- K921978: Breath Tracker (TM) Model 1800 Can-O-Gauge (Nov 17, 1992)
- K892942: Breath Tracker (Jun 23, 1989)

Source page: https://510kreport.com/company/core-m