Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of TeleflexLabelled 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 Rusch, Inc. with 26 510(k) clearances. The most recent is a 510(k) clearance dated May 9, 2001: RUSCH MMG/O'NEIL CATHETER.
| Date | Record | Source |
|---|---|---|
| May 9, 2001 | RUSCH MMG/O'NEIL CATHETERK010420 · FCM | 510(k) clearances |
| May 31, 2000 | RUSCH EMERGENCY MASKK993528 · CBP | 510(k) clearances |
| Mar 24, 2000 | RUSCH MANUAL RESUSCITATOR BAGK993194 · BTM | 510(k) clearances |
| Jun 9, 1998 | RUSCH SILICONE FOLEY CATHETERK980870 · EZL | 510(k) clearances |
| Jan 27, 1998 | RUSCH SIMPLASTIC COUNCILL TIP CATHETERK974419 · EZL | 510(k) clearances |
| May 23, 1997 | RUSCH ENTERAL FEEDING TUBEK963779 · FPD | 510(k) clearances |
| Feb 7, 1997 | RUSCH SUPRAPUBIC TRAYK970021 · KOB | 510(k) clearances |
| Dec 17, 1996 | RUSCH SIMPLASTIC FOLEY CATHETERIZATION SETK963993 · FCM | 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
