VOLU-SOL ZENKERS FIXATIVE
K-Number: K822127 · 1982-08-05
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Device Summary
Frequently Asked Questions
What is the VOLU-SOL ZENKERS FIXATIVE?
VOLU-SOL ZENKERS FIXATIVE 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 K822127.
When did VOLU-SOL ZENKERS FIXATIVE receive FDA 510(k) clearance?
VOLU-SOL ZENKERS FIXATIVE received FDA 510(k) clearance on 1982-08-05, under 510(k) number K822127.
Who is the listed applicant for VOLU-SOL ZENKERS FIXATIVE?
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 ZENKERS FIXATIVE?
The FDA product code for VOLU-SOL ZENKERS FIXATIVE is IFH.
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.
Related Devices (Code: IFH)
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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