VITOFIT
K-Number: K821260 · 1982-06-23
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Device Summary
Frequently Asked Questions
What is the VITOFIT?
VITOFIT 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 K821260.
When did VITOFIT receive FDA 510(k) clearance?
VITOFIT received FDA 510(k) clearance on 1982-06-23, under 510(k) number K821260.
Who is the listed applicant for VITOFIT?
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 VITOFIT?
The FDA product code for VITOFIT 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.
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
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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