ABCO EXAMINATION LAMP (GOOSENECK TYPE)— 510(k) K800230

Name: FDA 510(k) clearance K800230
Creator: U.S. Food and Drug Administration
Published: 1980-02-26

Substantially Equivalent

Abco Dealers, Inc.

FDA 510(k) clearance K800230 for ABCO EXAMINATION LAMP (GOOSENECK TYPE), Substantially Equivalent on 1980-02-26. Applicant: Abco Dealers, Inc.. Device class: 1.

Clearance details

Applicant: Abco Dealers, Inc.
Product code: Code KZF
Device class: Class 1
Regulation: 21 CFR 880.6320
Advisory panel: General Hospital
Date received: 1980-02-05
Decision date: 1980-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, 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.