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FDA 510(k)

DRAGER MEDICAL AIR COMPRESSOR

K-Number: K951126 · 1995-03-24

ApplicantDrager, Inc.
Decision Date1995-03-24
Product CodeBTL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DRAGER MEDICAL AIR COMPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Drager, Inc.. It received FDA 510(k) clearance on 1995-03-24 under 510(k) number K951126. The device is classified under product code BTL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRAGER MEDICAL AIR COMPRESSOR?

DRAGER MEDICAL AIR COMPRESSOR is a medical device that received FDA 510(k) clearance on 1995-03-24. The listed applicant is Drager, Inc.. The 510(k) number is K951126.

When did DRAGER MEDICAL AIR COMPRESSOR receive FDA 510(k) clearance?

DRAGER MEDICAL AIR COMPRESSOR received FDA 510(k) clearance on 1995-03-24, under 510(k) number K951126.

Who is the listed applicant for DRAGER MEDICAL AIR COMPRESSOR?

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

What is the FDA product code for DRAGER MEDICAL AIR COMPRESSOR?

The FDA product code for DRAGER MEDICAL AIR COMPRESSOR is BTL.

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Other records listing Drager, 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.

K992608ATC OPTION FOR EVITA 2 DURA AND EVITA 4K984577DRAGER OXYLOG 2000K983219NEOFLOW OPTION MODEL NUMBERS 8413563, 8411900K982789MEDICAL AIR COMPRESSOR, MODEL # 8413419K980642EVITA 4 (8411900)K974176BABYLOG 8000 PLUS

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Related Devices (Code: BTL)

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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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