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FDA 510(k)

ARTERIAL DIAGNOSTIC UNIT (ADU)

K-Number: K770115 · 1977-02-01

ApplicantMedical Electronic Devices, Inc.
Decision Date1977-02-01
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARTERIAL DIAGNOSTIC UNIT (ADU) is the device name listed in this FDA 510(k) record. The listed applicant is Medical Electronic Devices, Inc.. It received FDA 510(k) clearance on 1977-02-01 under 510(k) number K770115. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTERIAL DIAGNOSTIC UNIT (ADU)?

ARTERIAL DIAGNOSTIC UNIT (ADU) is a medical device that received FDA 510(k) clearance on 1977-02-01. The listed applicant is Medical Electronic Devices, Inc.. The 510(k) number is K770115.

When did ARTERIAL DIAGNOSTIC UNIT (ADU) receive FDA 510(k) clearance?

ARTERIAL DIAGNOSTIC UNIT (ADU) received FDA 510(k) clearance on 1977-02-01, under 510(k) number K770115.

Who is the listed applicant for ARTERIAL DIAGNOSTIC UNIT (ADU)?

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

What is the FDA product code for ARTERIAL DIAGNOSTIC UNIT (ADU)?

The FDA product code for ARTERIAL DIAGNOSTIC UNIT (ADU) is DPW.

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Related Devices (Code: DPW)

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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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