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FDA 510(k)

ANEROID SPHYGMOMANOMETER

K-Number: K760655 · 1976-10-05

ApplicantAbco Dealers, Inc.
Decision Date1976-10-05
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

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 1976-10-05 under 510(k) number K760655. 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 SPHYGMOMANOMETER?

ANEROID SPHYGMOMANOMETER is a medical device that received FDA 510(k) clearance on 1976-10-05. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K760655.

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

ANEROID SPHYGMOMANOMETER received FDA 510(k) clearance on 1976-10-05, under 510(k) number K760655.

Who is the listed applicant for 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 ANEROID SPHYGMOMANOMETER?

The FDA product code for ANEROID SPHYGMOMANOMETER 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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