HERMLE Z230H— 510(k) K920207

Substantially Equivalent

Labnet Intl., Inc.

FDA 510(k) clearance K920207 for HERMLE Z230H, Substantially Equivalent on 1992-06-09. Applicant: Labnet Intl., Inc.. Device class: 2.

Clearance details

Applicant: Labnet Intl., Inc.
Product code: Code GKG
Device class: Class 2
Regulation: 21 CFR 864.6400
Advisory panel: Hematology
Date received: 1992-01-16
Decision date: 1992-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woodbridge, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GKG

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K955795 — MULTI-CENTRIFUGE1996-03-29
K930415 — MICROHEMATOCRIT ROTOR1993-03-23
K925863 — SPUNCRIT1993-02-05
K920759 — CRITSPIN MICRO-HEMATOCRIT1992-04-29

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