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 Advanced Instrumentations, Inc. with 17 510(k) clearances. The most recent is a 510(k) clearance dated Dec 8, 2017: CMS-2000 Central Monitoring System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Dec 8, 2017 | CMS-2000 Central Monitoring SystemK172966 · MHX | 510(k) clearances |
| Dec 1, 2017 | DUS-6000 Digital Ultrasonic Diagnostic Imaging SystemK172931 · IYO | 510(k) clearances |
| Aug 31, 2017 | DUS-7000 Digital Color Doppler Ultrasound SystemK172055 · IYN | 510(k) clearances |
| Nov 19, 2014 | FM-3000 FETAL MONITORK141194 · HGM | 510(k) clearances |
| Apr 23, 2014 | PATIENT MONITORK132077 · MHX | 510(k) clearances |
| Oct 25, 2013 | DIAGNOSTIC ULTRASOUND SYSTEMK132059 · IYN | 510(k) clearances |
| Jan 11, 2013 | PATIENT MONITOR MODELS PM-2000A, PM-2000A+, PM-2000A PROK123048 · MHX | 510(k) clearances |
| Jan 26, 2012 | AM-6000 ANESTHESIA MACHINEK120075 · BSZ | 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
