Product code JYL— Ear, Nose, Throat

FDA has cleared 5 devices under product code JYL between 1978 and 1984, filed by 3 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.

• 19841 clearance
• 19822 clearances
• 19782 clearances

• Kelleher Corp.2 clearances
• Edward Weck, Inc.2 clearances
• Imm Enterprises , Ltd.1 clearance

• K834188 — JAKOBI SURG. INSTRUMENTS #7 10/43Imm Enterprises , Ltd.·1984-03-06
• K822195 — MIRCOSURGICAL INSTRUMENTSKelleher Corp.·1982-08-25
• K822166 — MICROSURGICAL EAR HOOKKelleher Corp.·1982-08-20
• K780287 — DAY HEAR HOOKEdward Weck, Inc.·1978-02-27
• K772390 — DAY EAR HOOKEdward Weck, Inc.·1978-01-17