# Device Labs, Inc.

- Location (FDA's records): Medway, MA
- FDA decisions: 6 (1988–1993): 6 510(k) clearances
- Product codes: LJT (2), KMF (1), FOZ (1), FMI (1), FPA (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: 13 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K930632: Chemosite Implantable Drug Delivery (Dec 22, 1993)
- K904417: Chemosite Implantable Drug Delivery System (Dec 5, 1990)
- K902135: Percutaneous Introducer Kit (Aug 1, 1990)
- K901722: Chemosite (TM) Implantable Drug Delivery System (Jul 3, 1990)
- K883764: Intravascular Administration Set (Dec 19, 1988)
- K882064: LO-Core Needle (Jul 8, 1988)

Source page: https://510kreport.com/company/device-labs