AMMEL PATIENT EXAMINATION GLOVES— 510(k) K894502

Name: FDA 510(k) clearance K894502
Creator: U.S. Food and Drug Administration
Published: 1989-10-10

Substantially Equivalent

Mauricio Menconi

FDA 510(k) clearance K894502 for AMMEL PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1989-10-10. Applicant: Mauricio Menconi. Device class: 1.

Clearance details

Applicant: Mauricio Menconi
Product code: Code LYY
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1989-07-19
Decision date: 1989-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Argentina, AR

Download summary PDF View on FDA.gov ↗

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K894501 — AMMEL STERILE SURGEON'S GLOVES1989-08-10

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