FDA Device Establishments · JSON-LD · Markdown
FEI 1219738 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 1219738 |
|---|---|
| Owner / Operator | KMC Systems (#9024188) |
| Address | 220 DANIEL WEBSTER HWY., Merrimack, NH, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 3 |
| Product codes (top 20) | GGN, JPA, DAP |
| Regulation § (21 CFR) | 864.5425, 864.7320 |
| Proprietary names | ACUSTAR |
Source: openFDA. Public-domain (CC0).