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 14, 2026, FDA's public records list Mennen Greatbatch Electronics with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 22, 1977: ECG TELEMETRY SYSTEM.
| Nov 22, 1977 | ECG TELEMETRY SYSTEMK772000 · DRG | 510(k) clearances |
| Jun 3, 1977 | PORTASCOPE IIK770832 · DPS | 510(k) clearances |
| Feb 24, 1977 | MONITOR, PORTABLE, PART #431-010K770279 · DXJ | 510(k) clearances |
| Feb 14, 1977 | ABDOMINAL FETAL ECG MODULEK770245 · KXN | 510(k) clearances |
| Feb 14, 1977 | ISOLATED EEG AMPLIFIER MODULEK770246 · GWQ | 510(k) clearances |
| Feb 14, 1977 | D.C. AMPLIFIER MODULEK770247 · DRQ | 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
