Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Namic with 8 510(k) clearances. The most recent is a 510(k) clearance dated Mar 29, 1996: BREEZE DIGITAL INFLATION DEVICE.
| Mar 29, 1996 | BREEZE DIGITAL INFLATION DEVICEK953676 · MAV | 510(k) clearances |
| Mar 25, 1996 | PERCEPTOR COMPENSATOR MORSE MANIFOLDK951722 · DRS | 510(k) clearances |
| Jul 9, 1993 | MORSE ANESTHESIA MANIFOLDK921322 · FPA | 510(k) clearances |
| Aug 24, 1982 | HIGH PRESSURE CONTRAST INJECTION LINEK822100 · DQO | 510(k) clearances |
| Jan 12, 1982 | CONTINUOUS FLUSH DEVICEK813549 · DRS | 510(k) clearances |
| Jan 25, 1979 | CATHETER, ARTERIAL LINEK790083 · DQY | 510(k) clearances |
| Jan 25, 1979 | ARTERIAL EXTENSION SETK790082 · DQO | 510(k) clearances |
| Jan 23, 1979 | STOPCOCKS, MANIFOLDSK782095 · DTL | 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
