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 J-Lloyd Medical, Inc. with 16 510(k) clearances. The most recent is a 510(k) clearance dated Apr 20, 1998: HEXAPOLAR ELECTRODE BALLOON FLOTATION CATHETER.
| Apr 20, 1998 | HEXAPOLAR ELECTRODE BALLOON FLOTATION CATHETERK971504 · DRF | 510(k) clearances |
| Apr 20, 1998 | ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC.K973639 · DRF | 510(k) clearances |
| Feb 13, 1998 | EMBOLECTOMY, IRRIGATION - OCCLUSION BALLOON CATHETER BY J-LLOYD MEDICAL, INC.K974335 · DXE | 510(k) clearances |
| Feb 13, 1998 | CHOLANGIOGRAPH BALLOON CATHETER BY J-LLOYD MEDICAL, INC.K974336 · GCJ | 510(k) clearances |
| Feb 3, 1997 | FLOW DIRECTED THERMODILUTION/INFUSION BALLOON CATHETER (575-110P)K963248 · DYG | 510(k) clearances |
| Sep 15, 1995 | DUAL FUNCTION PACING WEDGE PRESSURE BALLOON CATHETER BY J-LLOYDK950440 · DQO | 510(k) clearances |
| Aug 11, 1994 | FLOW DIRECT THERMODILUT BALLOON CATH HEPARIN COATEDK940547 · DYG | 510(k) clearances |
| Jul 25, 1994 | ARTERIAL EMBOLECTOMYK935405 · DXE | 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
