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FDA 510(k)

MODIFIED EXTRAVAKIT

K-Number: K882025 · 1988-07-27

ApplicantExtravakit, Inc.
Decision Date1988-07-27
Product CodeFMF
Advisory CommitteeHO
DecisionUnknown

Device Summary

MODIFIED EXTRAVAKIT is the device name listed in this FDA 510(k) record. The listed applicant is Extravakit, Inc.. It received FDA 510(k) clearance on 1988-07-27 under 510(k) number K882025. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MODIFIED EXTRAVAKIT?

MODIFIED EXTRAVAKIT is a medical device that received FDA 510(k) clearance on 1988-07-27. The listed applicant is Extravakit, Inc.. The 510(k) number is K882025.

When did MODIFIED EXTRAVAKIT receive FDA 510(k) clearance?

MODIFIED EXTRAVAKIT received FDA 510(k) clearance on 1988-07-27, under 510(k) number K882025.

Who is the listed applicant for MODIFIED EXTRAVAKIT?

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

What is the FDA product code for MODIFIED EXTRAVAKIT?

The FDA product code for MODIFIED EXTRAVAKIT is FMF.

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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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