Product code BXH— Anesthesiology

FDA has cleared 4 devices under product code BXH between 1977 and 1994, 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.

• 19941 clearance
• 19851 clearance
• 19841 clearance
• 19771 clearance

• Hospitak, Inc.1 clearance
• Erie Medical1 clearance
• Dynatech Cryomedical Co.1 clearance
• B & F Medical Products, Inc.1 clearance

• K942645 — B&F MEDICAL OXYGEN REG MECICAL OXY COMPRESS GAS REGB & F Medical Products, Inc.·1994-07-27
• K853040 — PRESSURE GAUGEErie Medical·1985-10-10
• K843212 — LOW PRESSURE ALARM FOR OXYGEN CYLINDERHospitak, Inc.·1984-09-19
• K770614 — MONITOR, GAS MANIFOLDDynatech Cryomedical Co.·1977-04-07