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., part of PhilipsLabelled 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 15, 2026, FDA's public records list Respironics New Jersey, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Aug 9, 2011: OPTICHAMBER DIAMOND VALVED HOLDING CHAMBER.
| Aug 9, 2011 | OPTICHAMBER DIAMOND VALVED HOLDING CHAMBERK110293 · NVP | 510(k) clearances |
| Jun 29, 2010 | LITETOUCH MASKK100285 · CAF | 510(k) clearances |
| Sep 12, 2007 | OPTICHAMBER ADVANTAGE ANTI-STATIC VALVED HOLDING CHAMBERK072418 · CAF | 510(k) clearances |
| Dec 20, 2005 | MYNEB NEBULIZER, MODEL RDD100K053203 · CAF | 510(k) clearances |
| Oct 13, 2004 | INSPIRATION ELITE NEBULIZER COMPRESSOR, WITH NEBULIZER, MODEL HS456K042655 · CAF | 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
