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FDA 510(k)

SPHYGMOMANOMETER

K-Number: K760157 · 1976-07-19

ApplicantEyvirco
Decision Date1976-07-19
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SPHYGMOMANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Eyvirco. It received FDA 510(k) clearance on 1976-07-19 under 510(k) number K760157. 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 SPHYGMOMANOMETER?

SPHYGMOMANOMETER is a medical device that received FDA 510(k) clearance on 1976-07-19. The listed applicant is Eyvirco. The 510(k) number is K760157.

When did SPHYGMOMANOMETER receive FDA 510(k) clearance?

SPHYGMOMANOMETER received FDA 510(k) clearance on 1976-07-19, under 510(k) number K760157.

Who is the listed applicant for SPHYGMOMANOMETER?

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

What is the FDA product code for SPHYGMOMANOMETER?

The FDA product code for SPHYGMOMANOMETER is DXQ.

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Related Devices (Code: DXQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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