Product code JZB— Ear, Nose, Throat

FDA has cleared 4 devices under product code JZB between 1982 and 1991, 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.

• 19911 clearance
• 19871 clearance
• 19841 clearance
• 19821 clearance

• Treace Medical, Inc.1 clearance
• Microtek Medical, Inc.1 clearance
• Kelleher Corp.1 clearance
• E.I. Dupont DE Nemours & Co., Inc.1 clearance

• K914226 — ACA(R) BETA-2-MICROGLOBULIN (B2M) TEST PACKE.I. Dupont DE Nemours & Co., Inc.·1991-11-19
• K870756 — VEIN GRAFT EAR SCISSORSTreace Medical, Inc.·1987-03-03
• K833603 — SCISSORS SHEA BELLUCCMicrotek Medical, Inc.·1984-01-03
• K822196 — EAR SCISSORSKelleher Corp.·1982-08-30