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 13, 2026, FDA's public records list Zcv, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Feb 1, 2001: ZYNERGY Z3K BALLOON GUIDED PACING AND MONITORING CATHETER.
| Date | Record | Source |
|---|---|---|
| Feb 1, 2001 | ZYNERGY Z3K BALLOON GUIDED PACING AND MONITORING CATHETERK010099 · LDF | 510(k) clearances |
| Jan 8, 2001 | ZYNERGY BALLOONPACE BALLOON GUIDED PACING AND MONITORING CATHETERK002603 · LDF | 510(k) clearances |
| Dec 20, 2000 | Z2 BALLOON GUIDED PACING & PRESSURE MONITORING CATHETER, MODEL Z2-7-02-1-10-0K003118 · DYG | 510(k) clearances |
| Dec 7, 2000 | ZYNERGY FEATHERPACE TRANSVENOUS BIPOLAR CATHETER, MODEL 04-X-02-3-10-3K002481 · LDF | 510(k) clearances |
| Apr 6, 2000 | ZYNERGY ZOLUTION ELECTROPHYSIOLOGY CATHETER, MODEL Z50000K991060 · DRF | 510(k) clearances |
| Sep 3, 1999 | ZYNERGY LOCK-SURE SINGLE PASS DRAINAGE CATHETER, Z10005/7/9K990689 · LJE | 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
