KNIFE HANDLE— 510(k) K822203

Substantially Equivalent

Kelleher Corp.

FDA 510(k) clearance K822203 for KNIFE HANDLE, Substantially Equivalent on 1982-08-20. Applicant: Kelleher Corp.. Device class: 1.

Clearance details

Applicant: Kelleher Corp.
Product code: Code KTG
Device class: Class 1
Regulation: 21 CFR 874.4420
Advisory panel: Ear, Nose, Throat
Date received: 1982-07-23
Decision date: 1982-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KTG

K822205 — KNIVES, ENT1982-08-30
K822280 — ENT KNIFE HANDLES1982-08-30
K822279 — LANCETS FOR EAR SURGERY1982-08-25
K822187 — TONSIL DISSECTORS1982-08-24

More clearances from Kelleher Corp.

K822268 — NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH1983-01-28
K822618 — EMERGENCY TRACHEOSTOMY INSTRUMENT SET1983-01-28
K823083 — ELECTROSURGICAL UNIT1982-12-07
K822252 — ENT TREATMENT UNITS1982-11-22
K823111 — NYSTYMOGRAPH ACCESS1982-11-22

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