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FDA 510(k)

REVIVE

K-Number: K833244 · 1983-11-29

ApplicantAladdin Industries, Inc.
Decision Date1983-11-29
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

REVIVE is the device name listed in this FDA 510(k) record. The listed applicant is Aladdin Industries, Inc.. It received FDA 510(k) clearance on 1983-11-29 under 510(k) number K833244. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REVIVE?

REVIVE is a medical device that received FDA 510(k) clearance on 1983-11-29. The listed applicant is Aladdin Industries, Inc.. The 510(k) number is K833244.

When did REVIVE receive FDA 510(k) clearance?

REVIVE received FDA 510(k) clearance on 1983-11-29, under 510(k) number K833244.

Who is the listed applicant for REVIVE?

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

What is the FDA product code for REVIVE?

The FDA product code for REVIVE is BTM.

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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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