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FDA 510(k)

ONE HAND ANEROID SPHYGMOMANOMETER

K-Number: K821232 · 1982-05-25

ApplicantAbco Dealers, Inc.
Decision Date1982-05-25
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ONE HAND ANEROID SPHYGMOMANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Abco Dealers, Inc.. It received FDA 510(k) clearance on 1982-05-25 under 510(k) number K821232. 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 ONE HAND ANEROID SPHYGMOMANOMETER?

ONE HAND ANEROID SPHYGMOMANOMETER is a medical device that received FDA 510(k) clearance on 1982-05-25. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K821232.

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

ONE HAND ANEROID SPHYGMOMANOMETER received FDA 510(k) clearance on 1982-05-25, under 510(k) number K821232.

Who is the listed applicant for ONE HAND ANEROID SPHYGMOMANOMETER?

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

What is the FDA product code for ONE HAND ANEROID SPHYGMOMANOMETER?

The FDA product code for ONE HAND ANEROID SPHYGMOMANOMETER is 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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