Product code KAE— Ear, Nose, Throat

FDA has cleared 14 devices under product code KAE between 1978 and 1986, 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.

• 19861 clearance
• 19853 clearances
• 19843 clearances
• 19822 clearances
• 19811 clearance
• 19784 clearances

• Edward Weck, Inc.4 clearances
• Microtek Medical, Inc.3 clearances
• Artiberia3 clearances
• Treace Medical, Inc.2 clearances
• Downs Surgical , Ltd.1 clearance
• American V. Mueller1 clearance

• K853708 — LARYNGASCOPES, FORCEPS, MICRO SUCTION TUBE & REFLEDowns Surgical , Ltd.·1986-02-14
• K851775 — 19-790 TO 19-1042 DRESSING/SPONGE FORCEPSArtiberia·1985-06-11
• K851794 — 41-180 TO 41-246 VARIOUS NASAL FORCEPSArtiberia·1985-06-11
• K851795 — 41-250 TO 41-282 VARIOUS NASAL CUTTING FORCEPSArtiberia·1985-06-11
• K833608 — GOLD ALLIGATOR FORCEPSMicrotek Medical, Inc.·1984-01-11
• K833605 — CUPPED FORCEPSMicrotek Medical, Inc.·1984-01-03
• K833607 — MCGEE FORCEPSMicrotek Medical, Inc.·1984-01-03
• K822369 — MICRO & MINI-MICRO ALLIGATOR FORCEPSTreace Medical, Inc.·1982-09-09
• K822372 — OFFICE ECONO-FORCEPSTreace Medical, Inc.·1982-09-09
• K812895 — YARMO NASAL CARTILAGE SOFTENERAmerican V. Mueller·1981-11-02
• K772377 — HILDYARD POST NASAL FORCEPEdward Weck, Inc.·1978-01-17
• K772396 — ALLIGATOR CUP FORCEPSEdward Weck, Inc.·1978-01-17
• K772397 — COTTLE COLUMELLA FORCEPEdward Weck, Inc.·1978-01-17
• K772398 — COTTLE LOWER LATERAL FORCEPSEdward Weck, Inc.·1978-01-17