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FDA 510(k)

ANEROID SPHYGMOMANOMETER

K-Number: K990638 · 1999-10-07

ApplicantGenmed, Inc.
Decision Date1999-10-07
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANEROID SPHYGMOMANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Genmed, Inc.. It received FDA 510(k) clearance on 1999-10-07 under 510(k) number K990638. 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 ANEROID SPHYGMOMANOMETER?

ANEROID SPHYGMOMANOMETER is a medical device that received FDA 510(k) clearance on 1999-10-07. The listed applicant is Genmed, Inc.. The 510(k) number is K990638.

When did ANEROID SPHYGMOMANOMETER receive FDA 510(k) clearance?

ANEROID SPHYGMOMANOMETER received FDA 510(k) clearance on 1999-10-07, under 510(k) number K990638.

Who is the listed applicant for ANEROID SPHYGMOMANOMETER?

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

What is the FDA product code for ANEROID SPHYGMOMANOMETER?

The FDA product code for ANEROID SPHYGMOMANOMETER 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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