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FDA 510(k)

ULTRAVIEW WAVEFORM PAGER SYSTEM, MODEL 91841

K-Number: K992749 · 2000-01-14

ApplicantSpacelabs Medical, Inc.
Decision Date2000-01-14
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ULTRAVIEW WAVEFORM PAGER SYSTEM, MODEL 91841 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 2000-01-14 under 510(k) number K992749. 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 ULTRAVIEW WAVEFORM PAGER SYSTEM, MODEL 91841?

ULTRAVIEW WAVEFORM PAGER SYSTEM, MODEL 91841 is a medical device that received FDA 510(k) clearance on 2000-01-14. The listed applicant is Spacelabs Medical, Inc.. The 510(k) number is K992749.

When did ULTRAVIEW WAVEFORM PAGER SYSTEM, MODEL 91841 receive FDA 510(k) clearance?

ULTRAVIEW WAVEFORM PAGER SYSTEM, MODEL 91841 received FDA 510(k) clearance on 2000-01-14, under 510(k) number K992749.

Who is the listed applicant for ULTRAVIEW WAVEFORM PAGER SYSTEM, MODEL 91841?

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 ULTRAVIEW WAVEFORM PAGER SYSTEM, MODEL 91841?

The FDA product code for ULTRAVIEW WAVEFORM PAGER SYSTEM, MODEL 91841 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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