FDA Device Establishments · JSON-LD · Markdown
FEI 3008436219 · Repack or Relabel Medical Device Manufacture Medical Device · Status: Active
| FEI Number | 3008436219 |
|---|---|
| Owner / Operator | JBC Corp (#10033382) |
| Address | 552 Central Drive, Suite No. 110, Virginia Beach, VA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | OHO |
| Regulation § (21 CFR) | 878.4014 |
| Proprietary names | Emergency Oxygen Kit (JBC-EOK-02); Medical Assault Kit (JBC-MAK-03-STD); CLS/Fanny Pack (JBC-FP/CLS-03-STD); SlimLine Trauma Pack (JBC-SLT-01); PIG Pack (JBC-PP-MSO-STD); SlimLine Combat Life Saver (JBC-SL/CLS-01); Disaster Response Trauma Kit (JBC-DRT-01); IV Catheter Exchange Kit (JBC-ISK-01); Suture Supply Kit (JBC-SSK-01) |
Source: openFDA. Public-domain (CC0).