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FDA 510(k)

ANEROID SPHYMOMANOMETER

K-Number: K792355 · 1979-12-05

ApplicantAbco Dealers, Inc.
Decision Date1979-12-05
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANEROID SPHYMOMANOMETER 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 1979-12-05 under 510(k) number K792355. 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 SPHYMOMANOMETER?

ANEROID SPHYMOMANOMETER is a medical device that received FDA 510(k) clearance on 1979-12-05. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K792355.

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

ANEROID SPHYMOMANOMETER received FDA 510(k) clearance on 1979-12-05, under 510(k) number K792355.

Who is the listed applicant for ANEROID SPHYMOMANOMETER?

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 SPHYMOMANOMETER?

The FDA product code for ANEROID SPHYMOMANOMETER 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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