Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of OlympusLabelled 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 Circon ACMI with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jan 18, 2002: USA SERIES LAPAROSCOPES.
| Jan 18, 2002 | USA SERIES LAPAROSCOPESK013165 · GCJ | 510(k) clearances |
| Nov 17, 1998 | AEH-3 ELECTROHYDRAULIC LITHOTRIPTER AND PROBES (E-1F, E-3F, E-5F, AND E-9F)K980492 · FFK | 510(k) clearances |
| Feb 28, 1991 | LAP 3501 HIGH FLOW INSUFFLATORK905705 · HIF | 510(k) clearances |
| Feb 28, 1991 | GYN-1500 HYSTEROSCOPIC INUFFLATORK905706 · HIG | 510(k) clearances |
| Apr 17, 1989 | MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPESK884097 · ODC | 510(k) clearances |
| Mar 3, 1989 | CIRCON ACMI BICAP II THERAPEUTIC SYSTEM BC-200K884025 · KNS | 510(k) clearances |
| Jan 11, 1989 | CIRCON ACMI BICAP III THERAPEUTIC SYSTEMK884254 · KNS | 510(k) clearances |
| Jan 10, 1989 | CIRCON ACMI BICAP HEMORRHOID SYSTEM BH-10 & BHP-20K884252 · KNS | 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
