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FDA 510(k)

VOLU-SOL HARRIS HEMATOXYLIN

K-Number: K800324 · 1980-02-22

Decision Date1980-02-22
Product CodeHYK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

VOLU-SOL HARRIS HEMATOXYLIN is the device name listed in this FDA 510(k) record. The listed applicant is Volu Sol Medical Industries. It received FDA 510(k) clearance on 1980-02-22 under 510(k) number K800324. The device is classified under product code HYK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOLU-SOL HARRIS HEMATOXYLIN?

VOLU-SOL HARRIS HEMATOXYLIN is a medical device that received FDA 510(k) clearance on 1980-02-22. The listed applicant is Volu Sol Medical Industries. The 510(k) number is K800324.

When did VOLU-SOL HARRIS HEMATOXYLIN receive FDA 510(k) clearance?

VOLU-SOL HARRIS HEMATOXYLIN received FDA 510(k) clearance on 1980-02-22, under 510(k) number K800324.

Who is the listed applicant for VOLU-SOL HARRIS HEMATOXYLIN?

The FDA 510(k) record lists Volu Sol Medical Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VOLU-SOL HARRIS HEMATOXYLIN?

The FDA product code for VOLU-SOL HARRIS HEMATOXYLIN is HYK.

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 Volu Sol Medical Industries 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 66 devices →

Related Devices (Code: HYK)

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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