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 13, 2026, FDA's public records list Ultramed, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 8, 1988: TRANSCRAN(TM) TRANSCRANIAL PULSED DOPPLER SYSTEM.
| Date | Record | Source |
|---|---|---|
| Sep 8, 1988 | TRANSCRAN(TM) TRANSCRANIAL PULSED DOPPLER SYSTEMK882015 · IYN | 510(k) clearances |
| Mar 2, 1988 | DOPPLEX ULTRASONIC DOPPLER SYSTEMK873989 · JOP | 510(k) clearances |
| Jul 7, 1986 | ULTRAMED TF 122 ULTRASON VASCU IMAG & DOPPLER SYSTK861378 · JOP | 510(k) clearances |
| Jun 23, 1986 | PHACOEMULSIFICATION ULTRASONIC FRAGMENT SYSTEMK862021 · HQC | 510(k) clearances |
| Apr 3, 1985 | PHACOEMULSIFICATION TIPK850578 · HQC | 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
