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FDA 510(k)

SPACELABS MEDICAL CLINICAL EVENT INTERFACE, MODEL 91847

K-Number: K062278 · 2006-09-19

ApplicantSpacelabs Medical, Inc.
Decision Date2006-09-19
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SPACELABS MEDICAL CLINICAL EVENT INTERFACE, MODEL 91847 is the device name listed in this FDA 510(k) record. The listed applicant is Spacelabs Medical, Inc.. It received FDA 510(k) clearance on 2006-09-19 under 510(k) number K062278. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPACELABS MEDICAL CLINICAL EVENT INTERFACE, MODEL 91847?

SPACELABS MEDICAL CLINICAL EVENT INTERFACE, MODEL 91847 is a medical device that received FDA 510(k) clearance on 2006-09-19. The listed applicant is Spacelabs Medical, Inc.. The 510(k) number is K062278.

When did SPACELABS MEDICAL CLINICAL EVENT INTERFACE, MODEL 91847 receive FDA 510(k) clearance?

SPACELABS MEDICAL CLINICAL EVENT INTERFACE, MODEL 91847 received FDA 510(k) clearance on 2006-09-19, under 510(k) number K062278.

Who is the listed applicant for SPACELABS MEDICAL CLINICAL EVENT INTERFACE, MODEL 91847?

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

What is the FDA product code for SPACELABS MEDICAL CLINICAL EVENT INTERFACE, MODEL 91847?

The FDA product code for SPACELABS MEDICAL CLINICAL EVENT INTERFACE, MODEL 91847 is MSX.

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Other records listing Spacelabs Medical, Inc. as applicant

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Related Devices (Code: MSX)

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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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