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FDA 510(k)

HERMLE Z230H

K-Number: K920207 · 1992-06-09

ApplicantLabnet Intl., Inc.
Decision Date1992-06-09
Product CodeGKG
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HERMLE Z230H is the device name listed in this FDA 510(k) record. The listed applicant is Labnet Intl., Inc.. It received FDA 510(k) clearance on 1992-06-09 under 510(k) number K920207. The device is classified under product code GKG. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HERMLE Z230H?

HERMLE Z230H is a medical device that received FDA 510(k) clearance on 1992-06-09. The listed applicant is Labnet Intl., Inc.. The 510(k) number is K920207.

When did HERMLE Z230H receive FDA 510(k) clearance?

HERMLE Z230H received FDA 510(k) clearance on 1992-06-09, under 510(k) number K920207.

Who is the listed applicant for HERMLE Z230H?

The FDA 510(k) record lists Labnet Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HERMLE Z230H?

The FDA product code for HERMLE Z230H is GKG.

Related Clinical Trials

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Related Devices (Code: GKG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K961803SPUNCRIT (MODEL DRC-40)Micro Diagnostics Corp.K955795MULTI-CENTRIFUGENovonx, Inc.K930415MICROHEMATOCRIT ROTORFisher Scientific Co., LLCK925863SPUNCRITbioMerieux, Inc.K920759CRITSPIN MICRO-HEMATOCRITStat-Spin TechnologiesK913128HEMATASTAT C-70BSeparation Technology, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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