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FDA 510(k)

ENDOBOY

K-Number: K033644 · 2004-03-24

ApplicantGeyser S.A.
Decision Date2004-03-24
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOBOY is the device name listed in this FDA 510(k) record. The listed applicant is Geyser S.A.. It received FDA 510(k) clearance on 2004-03-24 under 510(k) number K033644. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOBOY?

ENDOBOY is a medical device that received FDA 510(k) clearance on 2004-03-24. The listed applicant is Geyser S.A.. The 510(k) number is K033644.

When did ENDOBOY receive FDA 510(k) clearance?

ENDOBOY received FDA 510(k) clearance on 2004-03-24, under 510(k) number K033644.

Who is the listed applicant for ENDOBOY?

The FDA 510(k) record lists Geyser S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOBOY?

The FDA product code for ENDOBOY is GCJ.

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Related Devices (Code: GCJ)

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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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