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 MallinckrodtLabelled 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 National Catheter Co. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Apr 21, 1981: ANTHRON CATHETER SET.
| Apr 21, 1981 | ANTHRON CATHETER SETK802918 · FOZ | 510(k) clearances |
| Mar 13, 1981 | DOUBLE LUMEN TRACHEAL TUBEK802505 · BTR | 510(k) clearances |
| Mar 4, 1981 | REINFORCED TRACHEOSTOMY TUBE SET(TENTAT)K810321 · BTO | 510(k) clearances |
| Sep 9, 1980 | HI-LO TEMP GEN. PURPOSE TEMP. PROBEK801924 · FLL | 510(k) clearances |
| May 23, 1980 | MLT TUBE MICROLARYNGEAL TRACHEAL TUBE)K801005 · BTR | 510(k) clearances |
| Jul 6, 1979 | STETHOSCOPE WITH TEMPERATURE SENSORK791190 · BZT | 510(k) clearances |
| Dec 15, 1978 | TUBE, LEATHERMAN/IMBRUCEK781665 · GBA | 510(k) clearances |
| Apr 26, 1977 | MANIPULATOR & INJECTOR, UTERINEK770727 · KNA | 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
