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FDA 510(k)

ELECTRONIC HOUSE CALL

K-Number: K090801 · 2009-04-08

ApplicantExpress MD Solutions, LLC
Decision Date2009-04-08
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC HOUSE CALL is the device name listed in this FDA 510(k) record. The listed applicant is Express MD Solutions, LLC. It received FDA 510(k) clearance on 2009-04-08 under 510(k) number K090801. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRONIC HOUSE CALL?

ELECTRONIC HOUSE CALL is a medical device that received FDA 510(k) clearance on 2009-04-08. The listed applicant is Express MD Solutions, LLC. The 510(k) number is K090801.

When did ELECTRONIC HOUSE CALL receive FDA 510(k) clearance?

ELECTRONIC HOUSE CALL received FDA 510(k) clearance on 2009-04-08, under 510(k) number K090801.

Who is the listed applicant for ELECTRONIC HOUSE CALL?

The FDA 510(k) record lists Express MD Solutions, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRONIC HOUSE CALL?

The FDA product code for ELECTRONIC HOUSE CALL is DRG.

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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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