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 15, 2026, FDA's public records list Intersect Medical Products, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Nov 29, 1994: GAMGRO ENGSTROM Y FILTER WITH EDITH FLEX (1500 F), EDIT 500, 1000, 2600 AND Y FILTER PAC….
| Nov 29, 1994 | GAMGRO ENGSTROM Y FILTER WITH EDITH FLEX (1500 F), EDIT 500, 1000, 2600 AND Y FILTER PACKAGED ALONEK945543 · CAH | 510(k) clearances |
| Jan 9, 1980 | RESPIRATOR DISCONNECT ALARM CR 201K792516 · CAP | 510(k) clearances |
| Jan 9, 1980 | RESPIRATOR DISCONNECT ALARMK792515 · CAP | 510(k) clearances |
| Sep 19, 1979 | RESPIRATOR DISCONNECT ALARM CR201K791527 · CAP | 510(k) clearances |
| Sep 19, 1979 | RESPIRATOR DISCONNECT ALARM VA-100K791561 · CAP | 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
