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FDA 510(k)

MINICLINIC TM

K-Number: K771922 · 1977-11-02

ApplicantInstromedix, Inc.
Decision Date1977-11-02
Product CodeDTC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINICLINIC TM is the device name listed in this FDA 510(k) record. The listed applicant is Instromedix, Inc.. It received FDA 510(k) clearance on 1977-11-02 under 510(k) number K771922. The device is classified under product code DTC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINICLINIC TM?

MINICLINIC TM is a medical device that received FDA 510(k) clearance on 1977-11-02. The listed applicant is Instromedix, Inc.. The 510(k) number is K771922.

When did MINICLINIC TM receive FDA 510(k) clearance?

MINICLINIC TM received FDA 510(k) clearance on 1977-11-02, under 510(k) number K771922.

Who is the listed applicant for MINICLINIC TM?

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 MINICLINIC TM?

The FDA product code for MINICLINIC TM is DTC.

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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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