EXTRAVAKIT
K-Number: K874807 · 1988-02-04
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Device Summary
Frequently Asked Questions
What is the EXTRAVAKIT?
EXTRAVAKIT is a medical device that received FDA 510(k) clearance on 1988-02-04. The listed applicant is Cancer Technologies, Inc.. The 510(k) number is K874807.
When did EXTRAVAKIT receive FDA 510(k) clearance?
EXTRAVAKIT received FDA 510(k) clearance on 1988-02-04, under 510(k) number K874807.
Who is the listed applicant for EXTRAVAKIT?
The FDA 510(k) record lists Cancer Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EXTRAVAKIT?
The FDA product code for EXTRAVAKIT is FMF.
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 Cancer Technologies, 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: FMF)
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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