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FDA 510(k)

NARKOMED 6000

K-Number: K993826 · 2000-03-23

ApplicantDraeger Medical, Inc.
Decision Date2000-03-23
Product CodeMLC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NARKOMED 6000 is the device name listed in this FDA 510(k) record. The listed applicant is Draeger Medical, Inc.. It received FDA 510(k) clearance on 2000-03-23 under 510(k) number K993826. The device is classified under product code MLC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NARKOMED 6000?

NARKOMED 6000 is a medical device that received FDA 510(k) clearance on 2000-03-23. The listed applicant is Draeger Medical, Inc.. The 510(k) number is K993826.

When did NARKOMED 6000 receive FDA 510(k) clearance?

NARKOMED 6000 received FDA 510(k) clearance on 2000-03-23, under 510(k) number K993826.

Who is the listed applicant for NARKOMED 6000?

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

What is the FDA product code for NARKOMED 6000?

The FDA product code for NARKOMED 6000 is MLC.

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Other records listing Draeger Medical, Inc. as applicant

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Related Devices (Code: MLC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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