ELECTRO-ACUSCOPE 85— 510(k) K883911

Name: FDA 510(k) clearance K883911
Creator: U.S. Food and Drug Administration
Published: 1990-02-02

Substantially Equivalent

Biomedical Design Instruments

FDA 510(k) clearance K883911 for ELECTRO-ACUSCOPE 85, Substantially Equivalent on 1990-02-02. Applicant: Biomedical Design Instruments. Device class: 2.

Clearance details

Applicant: Biomedical Design Instruments
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1988-09-15
Decision date: 1990-02-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, US

Download summary PDF View on FDA.gov ↗

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