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 Carmel Pharma AB with 7 510(k) clearances. The most recent is a 510(k) clearance dated Apr 12, 2011: INFUSION ADAPTER C100.
| Apr 12, 2011 | INFUSION ADAPTER C100K110023 · LHI | 510(k) clearances |
| Dec 7, 2009 | INJECTOR LUER, MODEL N34, INJECTOR LUER LOCK, MODEL N35, INJECTOR LUER LOCK, N35C, CONNECTOR LUER LOCK, MODEL C35,K092782 · LHI | 510(k) clearances |
| Mar 23, 2009 | PHASEAL PROTECTOR P14, P21, P28 AND P50K090634 · LHI | 510(k) clearances |
| Apr 28, 2006 | PHASEAL - CLOSED SYSTEM FOR THE PREPARATION AND ADMINISTRATION OF PARENTERAL DRUGSK060866 · LHI | 510(k) clearances |
| Nov 15, 2002 | PHASEALK023747 · LHI | 510(k) clearances |
| May 12, 2000 | PROTECTOR 21, PROTECTOR 50, PROTECTOR 14, INJECTOR LUER LOCK, INFUSION ADAPTERK001368 · LHI | 510(k) clearances |
| Mar 3, 1998 | PHASEAL, CLOSED SYSTEM FORHANDLING OF PARENTERAL DRUGS, ADDITIONAL ADMINISTRATION DEVICES. C80 INFUSION ADAPTER, A10 PROK980381 · LHI | 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
