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FDA 510(k)

VOLU-SOL EA-50 STAIN

K-Number: K800322 · 1980-02-26

Decision Date1980-02-26
Product CodeHZJ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

VOLU-SOL EA-50 STAIN 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 1980-02-26 under 510(k) number K800322. The device is classified under product code HZJ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOLU-SOL EA-50 STAIN?

VOLU-SOL EA-50 STAIN is a medical device that received FDA 510(k) clearance on 1980-02-26. The listed applicant is Volu Sol Medical Industries. The 510(k) number is K800322.

When did VOLU-SOL EA-50 STAIN receive FDA 510(k) clearance?

VOLU-SOL EA-50 STAIN received FDA 510(k) clearance on 1980-02-26, under 510(k) number K800322.

Who is the listed applicant for VOLU-SOL EA-50 STAIN?

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 EA-50 STAIN?

The FDA product code for VOLU-SOL EA-50 STAIN is HZJ.

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: HZJ)

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

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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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