Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list RNK Products, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Oct 11, 2013: PPA/BT-RB STETHOSCOPE.
| Oct 11, 2013 | PPA/BT-RB STETHOSCOPEK132405 · DQD | 510(k) clearances |
| Oct 11, 2013 | PCP-USB STETHOSCOPEK132560 · DQD | 510(k) clearances |
| Jan 20, 2011 | PCP/PC STETHOSCOPEK102893 · DQD | 510(k) clearances |
| Jun 6, 2008 | TR-USB TELEPHONIC STETHOSCOPEK081032 · DQD | 510(k) clearances |
| Oct 26, 2007 | RNK ELECTRONIC STETHOSCOPEK072026 · DQD | 510(k) clearances |
| Mar 10, 2004 | RNK TELEPHONIC STETHOSCOPE, MODEL TR-1K034046 · DQD | 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
