AMPLAID A756 SCREENING ADMITTANCE METER— 510(k) K031978

Name: FDA 510(k) clearance K031978
Creator: U.S. Food and Drug Administration
Published: 2003-07-21

Substantially Equivalent

Amplaid

FDA 510(k) clearance K031978 for AMPLAID A756 SCREENING ADMITTANCE METER, Substantially Equivalent on 2003-07-21. Applicant: Amplaid. Device class: 2.

Clearance details

Applicant: Amplaid
Product code: Code ETY
Device class: Class 2
Regulation: 21 CFR 874.1090
Advisory panel: Ear, Nose, Throat
Date received: 2003-06-26
Decision date: 2003-07-21
Decision: Substantially Equivalent
Clearance type: Special
Location: Deer Field, IL, US

Download summary PDF View on FDA.gov ↗

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