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KCF — Dilator, Esophageal, Ent Class I

FDA Device Classification

Classification Details

Product Code
KCF
Device Class
Class I
Regulation Number
874.4420
Submission Type
Review Panel
EN
Medical Specialty
Ear, Nose, Throat
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K962688boston medical productsMONTGOMERY RADIOPAQUE SALIVARY BYPASS TUBEJuly 25, 1996
K923355boston medical productsPHARYNGEAL SALIVARY BYPASS TUBEOctober 6, 1992
K812305boston medical productsMONTG. ESOPHAGEAL -SALIVARY BYPASS- TUBESeptember 8, 1981