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FDA 510(k)

SYSMEX NE-1500, MODIFICATION

K-Number: K914744 · 1991-12-30

Decision Date1991-12-30
Product CodeGKZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SYSMEX NE-1500, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Toa Medical Electronics USA, Inc.. It received FDA 510(k) clearance on 1991-12-30 under 510(k) number K914744. The device is classified under product code GKZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYSMEX NE-1500, MODIFICATION?

SYSMEX NE-1500, MODIFICATION is a medical device that received FDA 510(k) clearance on 1991-12-30. The listed applicant is Toa Medical Electronics USA, Inc.. The 510(k) number is K914744.

When did SYSMEX NE-1500, MODIFICATION receive FDA 510(k) clearance?

SYSMEX NE-1500, MODIFICATION received FDA 510(k) clearance on 1991-12-30, under 510(k) number K914744.

Who is the listed applicant for SYSMEX NE-1500, MODIFICATION?

The FDA 510(k) record lists Toa Medical Electronics USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYSMEX NE-1500, MODIFICATION?

The FDA product code for SYSMEX NE-1500, MODIFICATION is GKZ.

Related Clinical Trials

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.

Other records listing Toa Medical Electronics USA, Inc. as applicant

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.

View all 33 devices →

Related Devices (Code: GKZ)

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.

Official Source

View on FDA Database →

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

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