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 Reimers Systems, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Aug 19, 2011: RSI 4200.
| Aug 19, 2011 | RSI 4200K102831 · CBF | 510(k) clearances |
| Oct 23, 1996 | ODS1 - HOOD DRIVERK962871 · CBF | 510(k) clearances |
| Oct 23, 1996 | GSP1 - GAS SELECTION PANELK962869 · CBF | 510(k) clearances |
| Dec 15, 1995 | T CLASS HYPERBARIC FACILITIESK954387 · CBF | 510(k) clearances |
| Jun 2, 1995 | LIFEFORCE CLINICAL HYPERBARIC FACILITYK951125 · CBF | 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
