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FDA 510(k)

VOLU-SOL SINGLE DIFFERENTIAL STAIN

K-Number: K822128 · 1982-08-05

Decision Date1982-08-05
Product CodeICN
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

VOLU-SOL SINGLE DIFFERENTIAL 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 1982-08-05 under 510(k) number K822128. The device is classified under product code ICN. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOLU-SOL SINGLE DIFFERENTIAL STAIN?

VOLU-SOL SINGLE DIFFERENTIAL STAIN is a medical device that received FDA 510(k) clearance on 1982-08-05. The listed applicant is Volu Sol Medical Industries. The 510(k) number is K822128.

When did VOLU-SOL SINGLE DIFFERENTIAL STAIN receive FDA 510(k) clearance?

VOLU-SOL SINGLE DIFFERENTIAL STAIN received FDA 510(k) clearance on 1982-08-05, under 510(k) number K822128.

Who is the listed applicant for VOLU-SOL SINGLE DIFFERENTIAL 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 SINGLE DIFFERENTIAL STAIN?

The FDA product code for VOLU-SOL SINGLE DIFFERENTIAL STAIN is ICN.

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: ICN)

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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