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FDA 510(k)

AS/3 ANESTHESIA MONTIOR WITH S-ANE99(A)/L-ARK99(A)

K-Number: K000815 · 2000-06-08

ApplicantDatex-Ohmeda
Decision Date2000-06-08
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AS/3 ANESTHESIA MONTIOR WITH S-ANE99(A)/L-ARK99(A) is the device name listed in this FDA 510(k) record. The listed applicant is Datex-Ohmeda. It received FDA 510(k) clearance on 2000-06-08 under 510(k) number K000815. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AS/3 ANESTHESIA MONTIOR WITH S-ANE99(A)/L-ARK99(A)?

AS/3 ANESTHESIA MONTIOR WITH S-ANE99(A)/L-ARK99(A) is a medical device that received FDA 510(k) clearance on 2000-06-08. The listed applicant is Datex-Ohmeda. The 510(k) number is K000815.

When did AS/3 ANESTHESIA MONTIOR WITH S-ANE99(A)/L-ARK99(A) receive FDA 510(k) clearance?

AS/3 ANESTHESIA MONTIOR WITH S-ANE99(A)/L-ARK99(A) received FDA 510(k) clearance on 2000-06-08, under 510(k) number K000815.

Who is the listed applicant for AS/3 ANESTHESIA MONTIOR WITH S-ANE99(A)/L-ARK99(A)?

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 AS/3 ANESTHESIA MONTIOR WITH S-ANE99(A)/L-ARK99(A)?

The FDA product code for AS/3 ANESTHESIA MONTIOR WITH S-ANE99(A)/L-ARK99(A) is MHX.

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Other records listing Datex-Ohmeda as applicant

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Related Devices (Code: MHX)

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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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