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FDA 510(k)

MEDDARS CARDIOVASCULAR DIAGNOSTIC SYSTEM

K-Number: K760767 · 1976-10-13

ApplicantHoneywell, Inc.
Decision Date1976-10-13
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDDARS CARDIOVASCULAR DIAGNOSTIC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1976-10-13 under 510(k) number K760767. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDDARS CARDIOVASCULAR DIAGNOSTIC SYSTEM?

MEDDARS CARDIOVASCULAR DIAGNOSTIC SYSTEM is a medical device that received FDA 510(k) clearance on 1976-10-13. The listed applicant is Honeywell, Inc.. The 510(k) number is K760767.

When did MEDDARS CARDIOVASCULAR DIAGNOSTIC SYSTEM receive FDA 510(k) clearance?

MEDDARS CARDIOVASCULAR DIAGNOSTIC SYSTEM received FDA 510(k) clearance on 1976-10-13, under 510(k) number K760767.

Who is the listed applicant for MEDDARS CARDIOVASCULAR DIAGNOSTIC SYSTEM?

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

What is the FDA product code for MEDDARS CARDIOVASCULAR DIAGNOSTIC SYSTEM?

The FDA product code for MEDDARS CARDIOVASCULAR DIAGNOSTIC SYSTEM is DQK.

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Related Devices (Code: DQK)

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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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