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 14, 2026, FDA's public records list McKinley, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Nov 8, 2004: BEELINE MOTIV, PROPOLIS, PCA.
| Nov 8, 2004 | BEELINE MOTIV, PROPOLIS, PCAK042228 · FRN | 510(k) clearances |
| Oct 7, 2003 | MODIFICATION TO: ACCUFUSER, ACCUFUSER PLUS, STANDARD PROCEDURE KITSK033039 · MEB | 510(k) clearances |
| Sep 23, 2003 | BEELINE SYSTEMK032642 · FRN | 510(k) clearances |
| Jul 1, 1999 | WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUSK991275 · FRN | 510(k) clearances |
| Jun 30, 1999 | MCKINLEY SP DISPOSABLE INFUSION PUMPK990461 · MEB | 510(k) clearances |
| Sep 30, 1998 | OUTBOUND DISPOSABLE SYRINGE INFUSER OUTBOUND 2 DISPOSABLE PUMPK982256 · MEB | 510(k) clearances |
| Jan 23, 1998 | MCKINLEY OUTBOUND-2 SYSTEMK971844 · FPA | 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
