Other-Sonic Transmission Gel
K-Number: K163023 · 2018-01-08
ApplicantPharmaceutical Innovations, Inc.
Decision Date2018-01-08
Product CodeMUI
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Other-Sonic Transmission Gel is a medical device manufactured by Pharmaceutical Innovations, Inc.. It received FDA 510(k) clearance on 2018-01-08 under approval number K163023. The device is classified under product code MUI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Other-Sonic Transmission Gel?
Other-Sonic Transmission Gel is a medical device that received FDA 510(k) clearance on 2018-01-08. It is manufactured by Pharmaceutical Innovations, Inc.. The 510(k) number is K163023.
When was Other-Sonic Transmission Gel approved by the FDA?
Other-Sonic Transmission Gel received FDA 510(k) clearance on 2018-01-08, under approval number K163023.
What company makes Other-Sonic Transmission Gel?
Other-Sonic Transmission Gel is manufactured by Pharmaceutical Innovations, Inc..
What is the FDA product code for Other-Sonic Transmission Gel?
The FDA product code for Other-Sonic Transmission Gel is MUI.
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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.