Product code EQL— Ear, Nose, Throat

FDA has cleared 8 devices under product code EQL between 1977 and 1999, filed by 7 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.

• 19991 clearance
• 19922 clearances
• 19891 clearance
• 19841 clearance
• 19821 clearance
• 19801 clearance
• 19771 clearance

• Kay Elemetrics Corp.2 clearances
• Richard Wolf Medical Instruments Corp.1 clearance
• Pentax Precision Instrument Corp.1 clearance
• Parke-Davis Co.1 clearance
• Kelleher Corp.1 clearance
• Jedmed Instrument Co.1 clearance
• Bruel & Kjaer Industri A/S1 clearance

• K984521 — RIWO DRIVE SYSTEM 2302 WITH GENERATOR, SMALL MOTOR HANDLES, 8563.111, 8563.351Richard Wolf Medical Instruments Corp.·1999-03-17
• K921184 — RLS 9100 RHINO-LARYNGEAL STROBOSCOPEKay Elemetrics Corp.·1992-05-28
• K921285 — 9105 RIGID TELESCOPIC ENDOSCOPEKay Elemetrics Corp.·1992-05-28
• K884933 — ENDOSTROBOSCOPE IVJedmed Instrument Co.·1989-02-15
• K842090 — RHINO-LARYNX STROBOSCOPE TYPE 4914Bruel & Kjaer Industri A/S·1984-07-18
• K822523 — LARYNGOSTROBOSCOPEKelleher Corp.·1982-09-09
• K801866 — PENTAX LARYNGO-STROBOSCOPE MODEL LS-1APentax Precision Instrument Corp.·1980-09-16
• K770466 — STOCKINGS, RVS TMParke-Davis Co.·1977-03-28