Product code KTG— Ear, Nose, Throat

ENT KNIFE HANDLES

Classification name: Knife, Ent
Device class: Class 1
Regulation: 21 CFR 874.4420
Advisory panel: Ear, Nose, Throat
Total cleared: 5
First cleared: 1982-08-20
Most recent: 1982-08-30

Market context for product code KTG

FDA has cleared 5 devices under product code KTG, all in 1982, filed by 1 applicant company. 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.

Top applicants under product code KTG

Kelleher Corp.5 clearances

Recent clearances under product code KTG

K822205 — KNIVES, ENTKelleher Corp.·1982-08-30
K822280 — ENT KNIFE HANDLESKelleher Corp.·1982-08-30
K822279 — LANCETS FOR EAR SURGERYKelleher Corp.·1982-08-25
K822187 — TONSIL DISSECTORSKelleher Corp.·1982-08-24
K822203 — KNIFE HANDLEKelleher Corp.·1982-08-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.