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 Accurate Surgical Instruments with 9 510(k) clearances. The most recent is a 510(k) clearance dated Dec 15, 1995: SWAN NECK PRESTERNAL PERITONEAL DIALYSIS CATHETER.
| Dec 15, 1995 | SWAN NECK PRESTERNAL PERITONEAL DIALYSIS CATHETERK950042 · FJS | 510(k) clearances |
| May 4, 1992 | INSERTIONK920515 · FJS | 510(k) clearances |
| Sep 19, 1991 | TROCAR (FALLER STYLET)K910786 · FJS | 510(k) clearances |
| Aug 22, 1991 | TITANIUM CATHETER EXTENDERK910785 · FJS | 510(k) clearances |
| Aug 15, 1991 | TITANIUM CONNECTOR (2 PART)K910787 · FKO | 510(k) clearances |
| Jun 19, 1986 | SWAN-NECK PERITONEAL DIALYSIS CATHETERSK862046 · FJS | 510(k) clearances |
| Jul 26, 1985 | STERILE CATHETERS-CATHETER PERITONEAL LONG-TERM INK850214 · FJS | 510(k) clearances |
| Dec 31, 1981 | CATHETER REGULARK813488 · FJS | 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
