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FDA 510(k)

A-V MINI CLINIC

K-Number: K800405 · 1980-07-21

ApplicantInstromedix, Inc.
Decision Date1980-07-21
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

A-V MINI CLINIC is the device name listed in this FDA 510(k) record. The listed applicant is Instromedix, Inc.. It received FDA 510(k) clearance on 1980-07-21 under 510(k) number K800405. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A-V MINI CLINIC?

A-V MINI CLINIC is a medical device that received FDA 510(k) clearance on 1980-07-21. The listed applicant is Instromedix, Inc.. The 510(k) number is K800405.

When did A-V MINI CLINIC receive FDA 510(k) clearance?

A-V MINI CLINIC received FDA 510(k) clearance on 1980-07-21, under 510(k) number K800405.

Who is the listed applicant for A-V MINI CLINIC?

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

What is the FDA product code for A-V MINI CLINIC?

The FDA product code for A-V MINI CLINIC is DRT.

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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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