Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwedenLabelled 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 Gibeck Respiration with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jun 24, 1988: HUMID-VENT FILTER.
| Jun 24, 1988 | HUMID-VENT FILTERK881657 · BYD | 510(k) clearances |
| Jun 16, 1988 | HUMID-VENT 2 S FLEXK881656 · BYD | 510(k) clearances |
| Jun 10, 1988 | HUMID-VENT 2 SK881644 · BYD | 510(k) clearances |
| Nov 24, 1987 | HUMID-VENT(R) 2 PORTK873768 · BYD | 510(k) clearances |
| Nov 6, 1987 | HUMID-VENT(R) MINIK873767 · BYD | 510(k) clearances |
| Aug 3, 1987 | STOM-VENTK872153 · BYD | 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
