Product code BXJ— Anesthesiology

FDA has cleared 4 devices under product code BXJ between 1976 and 1985, filed by 4 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 19851 clearance
• 19811 clearance
• 19771 clearance
• 19761 clearance

• Todd Industries, Inc.1 clearance
• Medipart Jerry Alexander1 clearance
• Inspiron Corp.1 clearance
• Bd Becton Dickinson Vacutainer Systems Preanalytic1 clearance

Other

1

Total

1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

• K853578 — MEDIPART DISPOS. NOSE CLIP MP-2001Medipart Jerry Alexander·1985-10-29
• K810339 — NOSECLIP #6118Todd Industries, Inc.·1981-03-17
• K770015 — NOSECLIP FOR RESP. CARE & PULMON. FUNC.Bd Becton Dickinson Vacutainer Systems Preanalytic·1977-03-16
• K760461 — NOSE CLIPInspiron Corp.·1976-08-26