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FDA 510(k)

ANEROID AND MERCURIAL SPHYGMOMANOMETERS

K-Number: K962655 · 1997-01-27

ApplicantAmerican Diagnostic Corp.
Decision Date1997-01-27
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANEROID AND MERCURIAL SPHYGMOMANOMETERS is the device name listed in this FDA 510(k) record. The listed applicant is American Diagnostic Corp.. It received FDA 510(k) clearance on 1997-01-27 under 510(k) number K962655. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANEROID AND MERCURIAL SPHYGMOMANOMETERS?

ANEROID AND MERCURIAL SPHYGMOMANOMETERS is a medical device that received FDA 510(k) clearance on 1997-01-27. The listed applicant is American Diagnostic Corp.. The 510(k) number is K962655.

When did ANEROID AND MERCURIAL SPHYGMOMANOMETERS receive FDA 510(k) clearance?

ANEROID AND MERCURIAL SPHYGMOMANOMETERS received FDA 510(k) clearance on 1997-01-27, under 510(k) number K962655.

Who is the listed applicant for ANEROID AND MERCURIAL SPHYGMOMANOMETERS?

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

What is the FDA product code for ANEROID AND MERCURIAL SPHYGMOMANOMETERS?

The FDA product code for ANEROID AND MERCURIAL SPHYGMOMANOMETERS is DXQ.

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Related Devices (Code: DXQ)

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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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