KAE — Forceps, Ent Class I

FDA Device Classification

FDA product code KAE covers "Forceps, Ent", a Class I medical device regulated under 21 CFR 874.4420. Submissions are reviewed by the Ear, Nose, Throat panel. At least 14 recent 510(k) clearances have been granted under this product code.

Classification details

Product Code
KAE
Device Class
Class I
Regulation Number
874.4420
Submission Type
510(k) Exempt
Review Panel
EN
Medical Specialty
Ear, Nose, Throat
Implant
No

Recent 510(k) clearances

K-NumberApplicantDevice NameDate
K853708Downs SurgicalLARYNGASCOPES, FORCEPS, MICRO SUCTION TUBE & REFLEFeb 14, 1986
K851795Artiberia41-250 TO 41-282 VARIOUS NASAL CUTTING FORCEPSJun 11, 1985
K851794Artiberia41-180 TO 41-246 VARIOUS NASAL FORCEPSJun 11, 1985
K851775Artiberia19-790 TO 19-1042 DRESSING/SPONGE FORCEPSJun 11, 1985
K833608Microtek MedicalGOLD ALLIGATOR FORCEPSJan 11, 1984
K833607Microtek MedicalMCGEE FORCEPSJan 3, 1984
K833605Microtek MedicalCUPPED FORCEPSJan 3, 1984
K822372Treace MedicalOFFICE ECONO-FORCEPSSep 9, 1982
K822369Treace MedicalMICRO & MINI-MICRO ALLIGATOR FORCEPSSep 9, 1982
K812895American V. MuellerYARMO NASAL CARTILAGE SOFTENERNov 2, 1981
K772396Edward WeckALLIGATOR CUP FORCEPSJan 17, 1978
K772398Edward WeckCOTTLE LOWER LATERAL FORCEPSJan 17, 1978
K772397Edward WeckCOTTLE COLUMELLA FORCEPJan 17, 1978
K772377Edward WeckHILDYARD POST NASAL FORCEPJan 17, 1978

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.