Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of GetingeLabelled by claude-sonnet-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 Sonicaid with 18 510(k) clearances. The most recent is a 510(k) clearance dated Feb 26, 1988: BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL.
| Date | Record | Source |
|---|---|---|
| Feb 26, 1988 | BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONALK873673 · DPT | 510(k) clearances |
| Aug 25, 1987 | 5 MHZ TRANSDUCERK872074 · JOP | 510(k) clearances |
| May 6, 1987 | VASOPULSE(TM)/MODEL 5000K863803 · JOM | 510(k) clearances |
| Nov 17, 1986 | VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBESK862720 · DPW | 510(k) clearances |
| Jul 14, 1986 | VASOVIEW DUPLEX IMAGING SYSTEMK861237 · ITX | 510(k) clearances |
| May 16, 1985 | VASOSCREEN IMPEDANCE PLETHYSMOGRAPHK851102 · DQB | 510(k) clearances |
| Jan 27, 1984 | VASOSCANK833902 · JOP | 510(k) clearances |
| Dec 1, 1983 | PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPHK832374 · JOM | 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
