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FDA 510(k)

RESUSIKIT

K-Number: K861482 · 1986-06-17

ApplicantBegley Enterprises, Inc.
Decision Date1986-06-17
Product CodeCAE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESUSIKIT is the device name listed in this FDA 510(k) record. The listed applicant is Begley Enterprises, Inc.. It received FDA 510(k) clearance on 1986-06-17 under 510(k) number K861482. The device is classified under product code CAE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESUSIKIT?

RESUSIKIT is a medical device that received FDA 510(k) clearance on 1986-06-17. The listed applicant is Begley Enterprises, Inc.. The 510(k) number is K861482.

When did RESUSIKIT receive FDA 510(k) clearance?

RESUSIKIT received FDA 510(k) clearance on 1986-06-17, under 510(k) number K861482.

Who is the listed applicant for RESUSIKIT?

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

What is the FDA product code for RESUSIKIT?

The FDA product code for RESUSIKIT is CAE.

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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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