BIOVATION DIGITAL URINOMETER— 510(k) K790862

Substantially Equivalent

Biovation, Inc.

FDA 510(k) clearance K790862 for BIOVATION DIGITAL URINOMETER, Substantially Equivalent on 1979-06-28. Applicant: Biovation, Inc.. Device class: 1.

Clearance details

Applicant: Biovation, Inc.
Product code: Code JRE
Device class: Class 1
Regulation: 21 CFR 862.2800
Advisory panel: Clinical Chemistry
Date received: 1979-05-07
Decision date: 1979-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code JRE

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K941906 — MODEL 2730 CLINICAL REFRACTOMETER1995-01-17
K941902 — MODEL 3471 CLINICAL REFRACTOMETER1994-12-13

More clearances from Biovation, Inc.

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K915071 — DIFFERENTIAL COUNTING BOARD1992-01-17
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.