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Percutaneous Atrial Catheter Kit
FDA product code OFK · Class 2 · Cardiovascular
125
Registered devices
67
Adverse events
2
Recalls
0
510(k) clearances
Devices with this code
VYGON — Vygon CorporationVYGON — Vygon CorporationVersaCross Connect Access Solution for POLARSHEATH — BOSTON SCIENTIFIC CORPORATIONVYGON — Vygon CorporationCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCVersaCross™ Access Solution — BOSTON SCIENTIFIC CORPORATIONCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCVersaCross Connect™ LAAC Access Solution — BOSTON SCIENTIFIC CORPORATIONCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCVYGON — Vygon CorporationVersaCross™ Access Solution — BOSTON SCIENTIFIC CORPORATIONCARDINAL HEALTH — Cardinal Health 200, LLCVersaCross™ Access Solution — BOSTON SCIENTIFIC CORPORATIONCARDINAL HEALTH — Cardinal Health 200, LLCVersaCross™ Access Solution — BOSTON SCIENTIFIC CORPORATIONCARDINAL HEALTH — Cardinal Health 200, LLCVersaCross™ Steerable Access Solution — BOSTON SCIENTIFIC CORPORATIONVersaCross™ Steerable Access Solution — BOSTON SCIENTIFIC CORPORATIONCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-04-21 | ARROW INTERNATIONAL, LLC | Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality iss |
| 2026-04-21 | ARROW INTERNATIONAL, LLC | Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality iss |
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