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 Maximum Performance Technologies (MPTS) with 11 510(k) clearances. The most recent is a 510(k) clearance dated Dec 10, 1991: CHALLENGE 3000 NEUROLOGICAL BOOSTER.
| Date | Record | Source |
|---|---|---|
| Dec 10, 1991 | CHALLENGE 3000 NEUROLOGICAL BOOSTERK903148 · IPF | 510(k) clearances |
| Oct 15, 1991 | CHALLENGE 4010 ONE CHANNEL WIDE PULSE STIMULATORK904360 · IPF | 510(k) clearances |
| Nov 5, 1990 | CHANLLENGE 1010 PATIENT KEY PROGRAM STATIONK903149 · IPF | 510(k) clearances |
| Aug 31, 1990 | CHALLENGE 6010 POWERED MUSCLE STIMULATORK902513 · IPF | 510(k) clearances |
| Aug 31, 1990 | CHALLENGE 7010 POWERED MUSCLE STIMULATORK902511 · IPF | 510(k) clearances |
| Aug 31, 1990 | CHALLENGE 5010 POWERED MUSCLE STIMULATORK902514 · IPF | 510(k) clearances |
| Aug 31, 1990 | CHALLENGE 8000 POWERED MUSCLE STIMULATORK902512 · IPF | 510(k) clearances |
| Jul 3, 1990 | CHALLENGE 5000 POWERED MUSCLE STIMULATORK901768 · IPF | 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
