FDA applicant
Msb, Ltd.
FDA records 7 decisions for Msb, Ltd. (Marlborough, Wiltshire, GB) from 1994 to 1998: 7 510(k) clearances. Most are in product codes DRX (Electrode, Electrocardiograph) and GEI (Electrosurgical, Cutting & Coagulation &…). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Msb, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Msb, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Msb, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report