Ultra/Phonic Conductivity Gel
K-Number: K163024 · 2018-01-08
Device Summary
Frequently Asked Questions
What is the Ultra/Phonic Conductivity Gel?
Ultra/Phonic Conductivity Gel is a medical device that received FDA 510(k) clearance on 2018-01-08. The listed applicant is Pharmaceutical Innovations, Inc.. The 510(k) number is K163024.
When did Ultra/Phonic Conductivity Gel receive FDA 510(k) clearance?
Ultra/Phonic Conductivity Gel received FDA 510(k) clearance on 2018-01-08, under 510(k) number K163024.
Who is the listed applicant for Ultra/Phonic Conductivity Gel?
The FDA 510(k) record lists Pharmaceutical Innovations, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ultra/Phonic Conductivity Gel?
The FDA product code for Ultra/Phonic Conductivity Gel is MUI.
Other records listing Pharmaceutical Innovations, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MUI)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.