SEPTUM ELEVATOR— 510(k) K890365

Substantially Equivalent

Kinetic Medical Products

FDA 510(k) clearance K890365 for SEPTUM ELEVATOR, Substantially Equivalent on 1989-02-03. Applicant: Kinetic Medical Products. Device class: 1.

Clearance details

Applicant: Kinetic Medical Products
Product code: Code GEG
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1989-01-23
Decision date: 1989-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Erie, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GEG

K891894 — ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSE1989-04-12
K891899 — ELEVATORS, VARIOUS TYPES1989-04-12
K890230 — LIGATURE NEEDLES1989-01-27
K890253 — SURGICAL ELEVATOR1989-01-27
K872491 — 1.1 TWIST DRILLS AND 1.2 CORTICAL DRILLS1987-07-16

More clearances from Kinetic Medical Products

K890385 — MIDWIFERY/OBSTETRICAL FORCEPS1989-03-01
K890376 — VAGINAL SPECULUM1989-02-27
K890380 — CERVICAL BIOPSY FORCEPS1989-02-27
K890382 — COMPRESSION FORCEPS1989-02-27
K890387 — MALLEABLE PLACENTA CURETTE1989-02-27

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