CLEARVIEW CW-10— 510(k) K870210

Substantially Equivalent

Clearview Instruments, Inc.

FDA 510(k) clearance K870210 for CLEARVIEW CW-10, Substantially Equivalent on 1987-04-28. Applicant: Clearview Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Clearview Instruments, Inc.
Product code: Code GKR
Device class: Class 2
Regulation: 21 CFR 864.5620
Advisory panel: Hematology
Date received: 1987-01-20
Decision date: 1987-04-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stow, MA, 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.