Product code CAO— Anesthesiology

FDA has cleared 6 devices under product code CAO between 1976 and 1998, filed by 6 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

• 19981 clearance
• 19891 clearance
• 19881 clearance
• 19871 clearance
• 19861 clearance
• 19761 clearance

• Sheridan Catheter Corp.1 clearance
• Sharn, Inc.1 clearance
• Respironics, Inc.1 clearance
• Mckesson Corp.1 clearance
• Green Field Medical Sourcing, Inc.1 clearance
• Cranco Co.1 clearance

• K971348 — FASTTRACH SINGLE-PASS TRACHEAL/ESOPHAGEAL AIRWAY SYSTEMGreen Field Medical Sourcing, Inc.·1998-02-27
• K894032 — EVAC-TUBESharn, Inc.·1989-08-31
• K875226 — ESOPHAGEAL OBTURATOR/TRACHEAL TUBESheridan Catheter Corp.·1988-01-19
• K864200 — VETA/VENTED ESOPHAGEAL TUBE AIRWAYCranco Co.·1987-03-17
• K863172 — RESPIRONICS PTL REVIVEEASYRespironics, Inc.·1986-11-04
• K761195 — ESOPHAGEAL OBTURATION AIRWAYMckesson Corp.·1976-12-09