Hydris™ Oral Rinse

FDA 510(k) K163029 · Biopharm Consult, LLC

Substantially Equivalent

510(k) numberK163029

Submission

Device name
Hydris™ Oral Rinse
Applicant
Biopharm Consult, LLC
Henrico, VA, US
Received
October 31, 2016
Decision date
June 19, 2017
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LFD – Saliva, Artificial
Device class
Unclassified

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Questions and answers

When was Hydris™ Oral Rinse cleared by the FDA?

Hydris™ Oral Rinse (K163029) received a 510(k) decision of Substantially Equivalent on June 19, 2017, 231 days after the submission was received.

What is the product code of K163029?

The FDA product code is LFD – Saliva, Artificial, a Unclassified device.