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FDA 510(k)

DATEX-OHMEDA HMEF 500

K-Number: K021265 · 2002-08-30

ApplicantDatex-Ohmeda
Decision Date2002-08-30
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DATEX-OHMEDA HMEF 500 is the device name listed in this FDA 510(k) record. The listed applicant is Datex-Ohmeda. It received FDA 510(k) clearance on 2002-08-30 under 510(k) number K021265. 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 DATEX-OHMEDA HMEF 500?

DATEX-OHMEDA HMEF 500 is a medical device that received FDA 510(k) clearance on 2002-08-30. The listed applicant is Datex-Ohmeda. The 510(k) number is K021265.

When did DATEX-OHMEDA HMEF 500 receive FDA 510(k) clearance?

DATEX-OHMEDA HMEF 500 received FDA 510(k) clearance on 2002-08-30, under 510(k) number K021265.

Who is the listed applicant for DATEX-OHMEDA HMEF 500?

The FDA 510(k) record lists Datex-Ohmeda as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DATEX-OHMEDA HMEF 500?

The FDA product code for DATEX-OHMEDA HMEF 500 is CAH.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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