KVM BLOOD CELL COUNTER— 510(k) K884471

Substantially Equivalent

Kvm Instruments, Inc.

FDA 510(k) clearance K884471 for KVM BLOOD CELL COUNTER, Substantially Equivalent on 1988-12-27. Applicant: Kvm Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Kvm Instruments, Inc.
Product code: Code GKL
Device class: Class 2
Regulation: 21 CFR 864.5200
Advisory panel: Hematology
Date received: 1988-10-25
Decision date: 1988-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, 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.