CONTOUROGRAPH M-500— 510(k) K800591

Name: FDA 510(k) clearance K800591
Creator: U.S. Food and Drug Administration
Published: 1980-04-02

Substantially Equivalent

Bio-Tek Instruments, Inc.

FDA 510(k) clearance K800591 for CONTOUROGRAPH M-500, Substantially Equivalent on 1980-04-02. Applicant: Bio-Tek Instruments, Inc.. Device class: Unclassified.

Clearance details

Applicant: Bio-Tek Instruments, Inc.
Product code: Code LDK
Device class: Unclassified
Advisory panel: Unknown
Date received: 1980-03-17
Decision date: 1980-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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