FDA Device Establishments · JSON-LD · Markdown
FEI 3004421347 · Manufacture Medical Device · Status: Active
| FEI Number | 3004421347 |
|---|---|
| Owner / Operator | LGM INTERNATIONAL INC. (#9059951) |
| Address | 295 North Dr Ste A, Melbourne, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | PPM |
| Regulation § (21 CFR) | 864.4010 |
| Proprietary names | LIQUI-PREP SPECIAL PROCESSING KIT; LIQUI-PREP CYTOLOGY PROCESSING SYST |
Source: openFDA. Public-domain (CC0).