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FDA 510(k)

SOLAR 9000 ANESTHESIA INFORMATION MONITOR

K-Number: K954852 · 1996-05-29

ApplicantMarquette Electronics, Inc.
Decision Date1996-05-29
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SOLAR 9000 ANESTHESIA INFORMATION MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Marquette Electronics, Inc.. It received FDA 510(k) clearance on 1996-05-29 under 510(k) number K954852. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLAR 9000 ANESTHESIA INFORMATION MONITOR?

SOLAR 9000 ANESTHESIA INFORMATION MONITOR is a medical device that received FDA 510(k) clearance on 1996-05-29. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K954852.

When did SOLAR 9000 ANESTHESIA INFORMATION MONITOR receive FDA 510(k) clearance?

SOLAR 9000 ANESTHESIA INFORMATION MONITOR received FDA 510(k) clearance on 1996-05-29, under 510(k) number K954852.

Who is the listed applicant for SOLAR 9000 ANESTHESIA INFORMATION MONITOR?

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

What is the FDA product code for SOLAR 9000 ANESTHESIA INFORMATION MONITOR?

The FDA product code for SOLAR 9000 ANESTHESIA INFORMATION MONITOR is DSI.

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Other records listing Marquette Electronics, Inc. as applicant

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Related Devices (Code: DSI)

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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