Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled 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 Stockert Instrumente with 9 510(k) clearances. The most recent is a 510(k) clearance dated Sep 23, 2004: STOCKERT SCP RHYTHM.
| Sep 23, 2004 | STOCKERT SCP RHYTHMK042374 · DWA | 510(k) clearances |
| Jul 2, 2004 | STOCKERTIR PURGE CONTROL (APC) SYSTEMK041558 · DTW | 510(k) clearances |
| Aug 29, 2003 | STOCKERT CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMPK032213 · DWA | 510(k) clearances |
| Nov 21, 2002 | STOCKERT PEDIATRIC AORTIC CANNULAE, MODEL NUMBERS A272-15 THROUGH A272-35K023622 · DWF | 510(k) clearances |
| Oct 11, 2002 | STOCKERT CORONARY PERFUSION CANNULAEK022280 · DWF | 510(k) clearances |
| Oct 9, 2002 | STOCKERT V172-28 VENOUS FEMORAL CANNULAK022321 · DWF | 510(k) clearances |
| Sep 23, 2002 | STOCKERT CENTRIFUGAL PUMP CONSOLEK020571 · DTQ | 510(k) clearances |
| Feb 5, 2002 | CENTRIFUGAL PUMPK011838 · DWA | 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
