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FDA 510(k)

SERVO GUARD, MODEL 64 81 290 EH88E

K-Number: K030071 · 2004-04-26

ApplicantMaquet, Inc.
Decision Date2004-04-26
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SERVO GUARD, MODEL 64 81 290 EH88E is the device name listed in this FDA 510(k) record. The listed applicant is Maquet, Inc.. It received FDA 510(k) clearance on 2004-04-26 under 510(k) number K030071. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERVO GUARD, MODEL 64 81 290 EH88E?

SERVO GUARD, MODEL 64 81 290 EH88E is a medical device that received FDA 510(k) clearance on 2004-04-26. The listed applicant is Maquet, Inc.. The 510(k) number is K030071.

When did SERVO GUARD, MODEL 64 81 290 EH88E receive FDA 510(k) clearance?

SERVO GUARD, MODEL 64 81 290 EH88E received FDA 510(k) clearance on 2004-04-26, under 510(k) number K030071.

Who is the listed applicant for SERVO GUARD, MODEL 64 81 290 EH88E?

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

What is the FDA product code for SERVO GUARD, MODEL 64 81 290 EH88E?

The FDA product code for SERVO GUARD, MODEL 64 81 290 EH88E is CAH.

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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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