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FDA 510(k)

SMARTSIGNS MINPULSE

K-Number: K081572 · 2008-10-01

ApplicantHuntleigh Healthcare , Ltd.
Decision Date2008-10-01
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SMARTSIGNS MINPULSE is the device name listed in this FDA 510(k) record. The listed applicant is Huntleigh Healthcare , Ltd.. It received FDA 510(k) clearance on 2008-10-01 under 510(k) number K081572. 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 SMARTSIGNS MINPULSE?

SMARTSIGNS MINPULSE is a medical device that received FDA 510(k) clearance on 2008-10-01. The listed applicant is Huntleigh Healthcare , Ltd.. The 510(k) number is K081572.

When did SMARTSIGNS MINPULSE receive FDA 510(k) clearance?

SMARTSIGNS MINPULSE received FDA 510(k) clearance on 2008-10-01, under 510(k) number K081572.

Who is the listed applicant for SMARTSIGNS MINPULSE?

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

What is the FDA product code for SMARTSIGNS MINPULSE?

The FDA product code for SMARTSIGNS MINPULSE is DQA.

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Related Devices (Code: DQA)

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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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