The following data is part of a premarket notification filed by Pharmaceutical Innovations, Inc. with the FDA for Ultra/phonic Conductivity Gel.
| Device ID | K163024 |
| 510k Number | K163024 |
| Device Name: | Ultra/Phonic Conductivity Gel |
| Classification | Media, Coupling, Ultrasound |
| Applicant | PHARMACEUTICAL INNOVATIONS, INC. 897 FRELINGHUYSEN AVE. Newark, NJ 07114 |
| Contact | Shirley J. Bergman |
| Correspondent | Shirley J. Bergman PHARMACEUTICAL INNOVATIONS, INC. 897 FRELINGHUYSEN AVE. Newark, NJ 07114 |
| Product Code | MUI |
| CFR Regulation Number | 892.1570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-10-31 |
| Decision Date | 2018-01-08 |
| Summary: | summary |