This page includes the latest FDA filings for Liquipak Corp. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 1815703 |
| FEI Number | 1815703 |
| Name | LIQUIPAK CORP. |
| Owner & Operator | LIQUIPAK CORP. |
| Contact Address | 2205 MICHIGAN AVE. -- Alma MI 48801 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 2205 MICHIGAN AVE. Alma, MI 48801 US |
| Establishment Type | Repack or Relabel Medical Device |
Device Company | Device | Date |
|---|---|---|
LIQUIPAK CORP. | ReSURGE Instrument Cleaning Solution | 2014-12-02 |
LIQUIPAK CORP. | Prolystica 2X Concentrate Enzymatic Presoak and Cleaner | 2014-12-02 |
LIQUIPAK CORP. | Locobase Wound and Skin Emulsion | 2007-12-05 |
LIQUIPAK CORP. | Vesta-Syde Decontamination System | 2001-12-07 |
| NCAGE Code | 4F452 | LIQUIPAK CORPORATION |
| CAGE Code | 4F452 | LIQUIPAK CORPORATION |
| S.A.M. Registration | 4F452 [8790784] | LIQUIPAK CORPORATION |