ENT FORCEPS— 510(k) K822278

Substantially Equivalent

Kelleher Corp.

FDA 510(k) clearance K822278 for ENT FORCEPS, Substantially Equivalent on 1982-08-27. Applicant: Kelleher Corp.. Device class: 1.

Clearance details

Applicant: Kelleher Corp.
Product code: Code GEN
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1982-07-29
Decision date: 1982-08-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GEN

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K953962 — FORCEPS1995-09-08
K932385 — SUTURE REMOVING FORCEPS1993-08-06
K904723 — FORCEPS1991-07-26
K911159 — PALPATION PROBE1991-03-29

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.