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 15, 2026, FDA's public records list Klein-Baker Medical, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 29, 1997: NEO-CARE PERITONEAL DIALYSIS ADMINISTRATION SET.
| Sep 29, 1997 | NEO-CARE PERITONEAL DIALYSIS ADMINISTRATION SETK972731 · KDJ | 510(k) clearances |
| May 22, 1997 | NEO-CARE LUMBER PUNCTURE KITK970997 · MIA | 510(k) clearances |
| Apr 1, 1997 | NEO-PICCK970434 · LJS | 510(k) clearances |
| Dec 24, 1996 | NEO-CARE DUAL LUMEN UMBILICAL CATHETERK963972 · FOS | 510(k) clearances |
| Nov 6, 1996 | NEO-CARE CATHETERIZATION TRAYK963867 · FOZ | 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
