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FDA 510(k)

VOLU-SOL CARNOY FLUID

K-Number: K822126 · 1982-08-05

Decision Date1982-08-05
Product CodeIGM
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

VOLU-SOL CARNOY FLUID 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 K822126. The device is classified under product code IGM. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOLU-SOL CARNOY FLUID?

VOLU-SOL CARNOY FLUID 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 K822126.

When did VOLU-SOL CARNOY FLUID receive FDA 510(k) clearance?

VOLU-SOL CARNOY FLUID received FDA 510(k) clearance on 1982-08-05, under 510(k) number K822126.

Who is the listed applicant for VOLU-SOL CARNOY FLUID?

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 CARNOY FLUID?

The FDA product code for VOLU-SOL CARNOY FLUID is IGM.

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: IGM)

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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