DUNRICH TABLES— 510(k) K800756

Substantially Equivalent

Dunrich, Inc.

FDA 510(k) clearance K800756 for DUNRICH TABLES, Substantially Equivalent on 1980-04-16. Applicant: Dunrich, Inc.. Device class: 1.

Clearance details

Applicant: Dunrich, Inc.
Product code: Code ETF
Device class: Class 1
Regulation: 21 CFR 874.5300
Advisory panel: Ear, Nose, Throat
Date received: 1980-04-04
Decision date: 1980-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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