Product code CBL— Anesthesiology

FDA has cleared 5 devices under product code CBL between 1981 and 1992, filed by 5 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.

• 19921 clearance
• 19901 clearance
• 19861 clearance
• 19851 clearance
• 19811 clearance

• Molecular Products , Ltd.1 clearance
• Medipart Jerry Alexander1 clearance
• Gibeck, Inc.1 clearance
• Dentsply Intl.1 clearance
• Allied Healthcare Products, Inc.1 clearance

• K921803 — SOFNOLIME CARBON DIOXIDE ABSORBENTMolecular Products , Ltd.·1992-10-15
• K897171 — DISPOSABLE CO2 ABSORBER/EGibeck, Inc.·1990-03-13
• K860147 — CARBON DIOXIDE ABSORBENTSDentsply Intl.·1986-02-28
• K853571 — MEDIPART SODA LIME MP-3522Medipart Jerry Alexander·1985-10-29
• K811260 — BARALYME CO2 ABSORBENTAllied Healthcare Products, Inc.·1981-05-27