DAD 16S, DATA ACQUISTION DEVICE 16 CH. SERIES— 510(k) K883461

Name: FDA 510(k) clearance K883461
Creator: U.S. Food and Drug Administration
Published: 1988-11-30

Substantially Equivalent

Biohm, Inc.

FDA 510(k) clearance K883461 for DAD 16S, DATA ACQUISTION DEVICE 16 CH. SERIES, Substantially Equivalent on 1988-11-30. Applicant: Biohm, Inc.. Device class: 2.

Clearance details

Applicant: Biohm, Inc.
Product code: Code GYE
Device class: Class 2
Regulation: 21 CFR 882.1855
Advisory panel: Neurology
Date received: 1988-08-12
Decision date: 1988-11-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boulder, CO, 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.