BIOVATION NEPHELOMETER— 510(k) K792045

Substantially Equivalent

Biovation, Inc.

FDA 510(k) clearance K792045 for BIOVATION NEPHELOMETER, Substantially Equivalent on 1979-10-30. Applicant: Biovation, Inc.. Device class: 1.

Clearance details

Applicant: Biovation, Inc.
Product code: Code JQX
Device class: Class 1
Regulation: 21 CFR 862.2700
Advisory panel: Clinical Chemistry
Date received: 1979-10-12
Decision date: 1979-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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More clearances from Biovation, Inc.

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K853026 — BIOVATION MAX DATA MANAGEMENT SYSTEM1985-08-02
K842401 — CHEMISTRY CONSOLE1984-09-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.