Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Msb Ltd with 7 510(k) clearances. The most recent is a 510(k) clearance dated Feb 27, 1998: MSB TENS ELECTRODES (DISPOSABLE).
| Date | Record | Source |
|---|---|---|
| Feb 27, 1998 | MSB TENS ELECTRODES (DISPOSABLE)K980229 · GXY | 510(k) clearances |
| May 17, 1996 | UNILECT, MONITAB AND BIOTRACE-HRK944497 · DRX | 510(k) clearances |
| May 16, 1996 | BIOTRACE-N, NS, 410 AND RTK944496 · DRX | 510(k) clearances |
| Jan 30, 1996 | NEUTRALECT ADULT STANDARD, RETURN (REM) & PAEDIATRIC ELECTROSURGERY PLATE (MODIFICATION)K955261 · GEI | 510(k) clearances |
| Oct 16, 1995 | ECOTABSK950587 · DRX | 510(k) clearances |
| Jul 7, 1995 | ECG ELECTRODEK944260 · DRX | 510(k) clearances |
| Nov 9, 1994 | NEUTRALECT ADULT STANDARD, RETURN (REM), PAEDIATRIC STANDARD, RETURN (REM)K944817 · GEI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
