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 15, 2026, FDA's public records list Olsen Electrosurgical with 11 510(k) clearances. The most recent is a 510(k) clearance dated Apr 21, 1994: INSULATED SPECULUM W/ SMOKE EVACUATOR OPTION.
| Apr 21, 1994 | INSULATED SPECULUM W/ SMOKE EVACUATOR OPTIONK922154 · HIB | 510(k) clearances |
| Apr 15, 1992 | OLSEN LAPAROSCOPIC INSTR, DISPOSABLE, SINGLE USEK912611 · GEI | 510(k) clearances |
| Dec 23, 1991 | TEFLON COATED ELECTRODES/ELECTRODES HANDLESK913108 · GEI | 510(k) clearances |
| Nov 1, 1991 | SMOKE/ODOR EVACUATOR #757K912612 · FYD | 510(k) clearances |
| Jan 13, 1989 | 600 & 900 SERIES ELECTRODES & 755 & 756 HANDLEK885200 · GEI | 510(k) clearances |
| Jan 13, 1989 | #500 SERIES FORCEPS W/CUT/COAGULATE SWITCHESK885199 · GEI | 510(k) clearances |
| Oct 24, 1988 | MODIFIED OLSEN 755/756 SWITCHPENSK884174 · HAM | 510(k) clearances |
| Oct 24, 1988 | #820/821 BIPOLAR FORCEPSK884175 · HAM | 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
