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FDA 510(k)

VITASAN

K-Number: K821259 · 1982-06-23

ApplicantSelomas, Inc.
Decision Date1982-06-23
Product CodeFQL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITASAN is the device name listed in this FDA 510(k) record. The listed applicant is Selomas, Inc.. It received FDA 510(k) clearance on 1982-06-23 under 510(k) number K821259. The device is classified under product code FQL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITASAN?

VITASAN is a medical device that received FDA 510(k) clearance on 1982-06-23. The listed applicant is Selomas, Inc.. The 510(k) number is K821259.

When did VITASAN receive FDA 510(k) clearance?

VITASAN received FDA 510(k) clearance on 1982-06-23, under 510(k) number K821259.

Who is the listed applicant for VITASAN?

The FDA 510(k) record lists Selomas, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITASAN?

The FDA product code for VITASAN is FQL.

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 Selomas, Inc. 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 7 devices →

Related Devices (Code: FQL)

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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