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FDA 510(k)

DRAEGER MICRO2+ AND MASIMO MINISAT

K-Number: K032537 · 2003-11-25

ApplicantDraeger Medical Systems, Inc.
Decision Date2003-11-25
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DRAEGER MICRO2+ AND MASIMO MINISAT is the device name listed in this FDA 510(k) record. The listed applicant is Draeger Medical Systems, Inc.. It received FDA 510(k) clearance on 2003-11-25 under 510(k) number K032537. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRAEGER MICRO2+ AND MASIMO MINISAT?

DRAEGER MICRO2+ AND MASIMO MINISAT is a medical device that received FDA 510(k) clearance on 2003-11-25. The listed applicant is Draeger Medical Systems, Inc.. The 510(k) number is K032537.

When did DRAEGER MICRO2+ AND MASIMO MINISAT receive FDA 510(k) clearance?

DRAEGER MICRO2+ AND MASIMO MINISAT received FDA 510(k) clearance on 2003-11-25, under 510(k) number K032537.

Who is the listed applicant for DRAEGER MICRO2+ AND MASIMO MINISAT?

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

What is the FDA product code for DRAEGER MICRO2+ AND MASIMO MINISAT?

The FDA product code for DRAEGER MICRO2+ AND MASIMO MINISAT is DQA.

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Related Devices (Code: DQA)

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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