7-120, 7-130,7-140, 7-150,9-151 TO 168, 9-171 TO 1— 510(k) K851751

Name: FDA 510(k) clearance K851751
Creator: U.S. Food and Drug Administration
Published: 1985-06-20

Substantially Equivalent

Artiberia

FDA 510(k) clearance K851751 for 7-120, 7-130,7-140, 7-150,9-151 TO 168, 9-171 TO 1, Substantially Equivalent on 1985-06-20. Applicant: Artiberia. Device class: 1.

Clearance details

Applicant: Artiberia
Product code: Code GDX
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 ↗

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K851745 — 1-100 UNIVERSAL SET OTOSCOPE & LARYNX EXPLORATON B1985-08-29
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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.