BONE RONGEUR, SINGLE-ACTION— 510(k) K890255

Name: FDA 510(k) clearance K890255
Creator: U.S. Food and Drug Administration
Published: 1989-01-27

Substantially Equivalent

Kinetic Medical Products

FDA 510(k) clearance K890255 for BONE RONGEUR, SINGLE-ACTION, Substantially Equivalent on 1989-01-27. Applicant: Kinetic Medical Products. Device class: 1.

Clearance details

Applicant: Kinetic Medical Products
Product code: Code EMH
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1989-01-18
Decision date: 1989-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Erie, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EMH

view all

K890256 — BONE RONGEUR, DOUBLE-ACTION1989-01-27
K854887 — MANU/SURG INST/ACCESS WUERZBURG TIT MINI BONE PLAT1986-02-28
K851710 — 586 TO 596 VARIOUS TYPES DENTAL ROOT SPLINTER FORC1985-06-11
K834190 — JAKOBI SURG. INSTRUMENTS #8 151984-03-06
K834366 — SURGICAL INSTRUMENTS & ACCESSORIES1984-02-27

More clearances from Kinetic Medical Products

view all

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.