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FDA 510(k)

MPT 24 AND VITAL VIEW 24

K-Number: K000276 · 2000-03-01

ApplicantCriticare Systems, Inc.
Decision Date2000-03-01
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MPT 24 AND VITAL VIEW 24 is the device name listed in this FDA 510(k) record. The listed applicant is Criticare Systems, Inc.. It received FDA 510(k) clearance on 2000-03-01 under 510(k) number K000276. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MPT 24 AND VITAL VIEW 24?

MPT 24 AND VITAL VIEW 24 is a medical device that received FDA 510(k) clearance on 2000-03-01. The listed applicant is Criticare Systems, Inc.. The 510(k) number is K000276.

When did MPT 24 AND VITAL VIEW 24 receive FDA 510(k) clearance?

MPT 24 AND VITAL VIEW 24 received FDA 510(k) clearance on 2000-03-01, under 510(k) number K000276.

Who is the listed applicant for MPT 24 AND VITAL VIEW 24?

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

What is the FDA product code for MPT 24 AND VITAL VIEW 24?

The FDA product code for MPT 24 AND VITAL VIEW 24 is DRG.

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Other records listing Criticare Systems, 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.

K101602VITAL SIGNS MONITORK091050506CN PATIENT MONITORK0425698600 VITAL SIGNS MONITORK030613VITAL SIGNS MONITOR W/ARRHYTHMIA DETECTION AND ST ANALYSIS, MODEL 8100K022435507EL VITAL SIGNS MONITORK0120598100/8500 VITAL SIGNS MONITOR

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Related Devices (Code: DRG)

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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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