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FDA 510(k)

DRAGER BAROMED

K-Number: K840279 · 1984-03-02

ApplicantDraeger Medical, Inc.
Decision Date1984-03-02
Product CodeCAP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DRAGER BAROMED 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 1984-03-02 under 510(k) number K840279. The device is classified under product code CAP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRAGER BAROMED?

DRAGER BAROMED is a medical device that received FDA 510(k) clearance on 1984-03-02. The listed applicant is Draeger Medical, Inc.. The 510(k) number is K840279.

When did DRAGER BAROMED receive FDA 510(k) clearance?

DRAGER BAROMED received FDA 510(k) clearance on 1984-03-02, under 510(k) number K840279.

Who is the listed applicant for DRAGER BAROMED?

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 DRAGER BAROMED?

The FDA product code for DRAGER BAROMED is CAP.

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Other records listing Draeger Medical, Inc. as applicant

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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Related Devices (Code: CAP)

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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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