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FDA 510(k)

A.P.GRAPH III(TM) CARDIOVASCULAR ANALYZER

K-Number: K905114 · 1991-05-07

ApplicantResearch Consultants, Inc.
Decision Date1991-05-07
Product CodeJOM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

A.P.GRAPH III(TM) CARDIOVASCULAR ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Research Consultants, Inc.. It received FDA 510(k) clearance on 1991-05-07 under 510(k) number K905114. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A.P.GRAPH III(TM) CARDIOVASCULAR ANALYZER?

A.P.GRAPH III(TM) CARDIOVASCULAR ANALYZER is a medical device that received FDA 510(k) clearance on 1991-05-07. The listed applicant is Research Consultants, Inc.. The 510(k) number is K905114.

When did A.P.GRAPH III(TM) CARDIOVASCULAR ANALYZER receive FDA 510(k) clearance?

A.P.GRAPH III(TM) CARDIOVASCULAR ANALYZER received FDA 510(k) clearance on 1991-05-07, under 510(k) number K905114.

Who is the listed applicant for A.P.GRAPH III(TM) CARDIOVASCULAR ANALYZER?

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

What is the FDA product code for A.P.GRAPH III(TM) CARDIOVASCULAR ANALYZER?

The FDA product code for A.P.GRAPH III(TM) CARDIOVASCULAR ANALYZER is JOM.

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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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