Product code JYO— Ear, Nose, Throat

FDA has cleared 7 devices under product code JYO between 1978 and 1991, filed by 6 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
• 19843 clearances
• 19831 clearance
• 19782 clearances

• Edward Weck, Inc.2 clearances
• Treace Medical, Inc.1 clearance
• Sharpoint, Inc.1 clearance
• Premier Dental Products Co.1 clearance
• Microtek Medical, Inc.1 clearance
• Acoustic Imaging Technologies Corp.1 clearance

• K910212 — COLOR DOPPLER OPTION TO AI 5200 DIAG ULTRASO SYSTAcoustic Imaging Technologies Corp.·1991-07-11
• K841006 — EAR KNIFE-VARIOUSPremier Dental Products Co.·1984-05-30
• K840764 — EAR KNIVESSharpoint, Inc.·1984-05-21
• K833602 — ROLLER KNIFE-TRANSVERSE -SAGITTALMicrotek Medical, Inc.·1984-01-03
• K823911 — KNIFE BLADE TIPTreace Medical, Inc.·1983-01-21
• K772372 — ROLLER KNIFEEdward Weck, Inc.·1978-01-17
• K772384 — MYRINGOTOMY KNIFEEdward Weck, Inc.·1978-01-17