BMS-2000 MOBILE EEG SYSTEM— 510(k) K891405

Substantially Equivalent

Buckman Co., Inc.

FDA 510(k) clearance K891405 for BMS-2000 MOBILE EEG SYSTEM, Substantially Equivalent on 1989-08-02. Applicant: Buckman Co., Inc.. Device class: 2.

Clearance details

Applicant: Buckman Co., Inc.
Product code: Code GYE
Device class: Class 2
Regulation: 21 CFR 882.1855
Advisory panel: Neurology
Date received: 1989-03-14
Decision date: 1989-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Martinez, CA, 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.