9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS— 510(k) K851752

Name: FDA 510(k) clearance K851752
Creator: U.S. Food and Drug Administration
Published: 1985-06-20

Substantially Equivalent

Artiberia

FDA 510(k) clearance K851752 for 9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS, Substantially Equivalent on 1985-06-20. Applicant: Artiberia. Device class: 1.

Clearance details

Applicant: Artiberia
Product code: Code GDN
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1985-04-25
Decision date: 1985-06-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

More clearances from Artiberia

view all

K851745 — 1-100 UNIVERSAL SET OTOSCOPE & LARYNX EXPLORATON B1985-08-29
K851786 — 27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLF1985-07-09
K851718 — 930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTES1985-07-02
K851719 — 1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS1985-07-02
K851720 — 1155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS1985-07-02

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