Identifiers
- 510(k) Number
- K830947 FDA 510(k)
Classification
- Advisory Committee
- Unknown FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Syringe/Needle Dispos-Box-Cutter/Crimper by Post Medical, Inc. — 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 | K830947 | N/A | Active |
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Manufacturer
- Manufacturer
- Post Medical, Inc.
Sources (1)
- FDA 510(k) K830947 24 fields · synced Jun 18, 2026