← Back to catalogue
Tracheal Stent System (Y-Shaped)
FDA 510(k)Class II (US FDA 510(k))
510(k) K212403
Identifiers
- 510(k) Number
- K212403 FDA 510(k)
- FDA Product Code
- JCT FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 878.3720 FDA 510(k)
- Regulation Number
- 878.3720 FDA 510(k)
- Advisory Committee
- General, Plastic Surgery FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Tracheal Stent System (Y-Shaped) by Micro-Tech (Nanjing) Co., Ltd. — Class II — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K212403 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Micro-Tech (Nanjing) Co., Ltd.
Sources (1)
- FDA 510(k) K212403 24 fields · synced Jun 20, 2026