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FDA 510(k)

ACCUSTAT MODEL 102 NON-INVASIVE BLOOD MONITORING

K-Number: K881272 · 1988-06-22

ApplicantAccustat, Inc.
Decision Date1988-06-22
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ACCUSTAT MODEL 102 NON-INVASIVE BLOOD MONITORING is the device name listed in this FDA 510(k) record. The listed applicant is Accustat, Inc.. It received FDA 510(k) clearance on 1988-06-22 under 510(k) number K881272. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCUSTAT MODEL 102 NON-INVASIVE BLOOD MONITORING?

ACCUSTAT MODEL 102 NON-INVASIVE BLOOD MONITORING is a medical device that received FDA 510(k) clearance on 1988-06-22. The listed applicant is Accustat, Inc.. The 510(k) number is K881272.

When did ACCUSTAT MODEL 102 NON-INVASIVE BLOOD MONITORING receive FDA 510(k) clearance?

ACCUSTAT MODEL 102 NON-INVASIVE BLOOD MONITORING received FDA 510(k) clearance on 1988-06-22, under 510(k) number K881272.

Who is the listed applicant for ACCUSTAT MODEL 102 NON-INVASIVE BLOOD MONITORING?

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

What is the FDA product code for ACCUSTAT MODEL 102 NON-INVASIVE BLOOD MONITORING?

The FDA product code for ACCUSTAT MODEL 102 NON-INVASIVE BLOOD MONITORING is DXN.

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Related Devices (Code: DXN)

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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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