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FDA 510(k)

ARTRAC VITAL SIGNS MON. MODELS 7000 AND 5000 & ACC

K-Number: K904088 · 1991-02-05

ApplicantSentinel
Decision Date1991-02-05
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARTRAC VITAL SIGNS MON. MODELS 7000 AND 5000 & ACC is the device name listed in this FDA 510(k) record. The listed applicant is Sentinel. It received FDA 510(k) clearance on 1991-02-05 under 510(k) number K904088. 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 ARTRAC VITAL SIGNS MON. MODELS 7000 AND 5000 & ACC?

ARTRAC VITAL SIGNS MON. MODELS 7000 AND 5000 & ACC is a medical device that received FDA 510(k) clearance on 1991-02-05. The listed applicant is Sentinel. The 510(k) number is K904088.

When did ARTRAC VITAL SIGNS MON. MODELS 7000 AND 5000 & ACC receive FDA 510(k) clearance?

ARTRAC VITAL SIGNS MON. MODELS 7000 AND 5000 & ACC received FDA 510(k) clearance on 1991-02-05, under 510(k) number K904088.

Who is the listed applicant for ARTRAC VITAL SIGNS MON. MODELS 7000 AND 5000 & ACC?

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

What is the FDA product code for ARTRAC VITAL SIGNS MON. MODELS 7000 AND 5000 & ACC?

The FDA product code for ARTRAC VITAL SIGNS MON. MODELS 7000 AND 5000 & ACC is DQA.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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