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Sterile Polyisoprene Powder Free Surgical Glove, Tested for Use with Chemothera…
FDA 510(k)Class I (US FDA 510(k))
510(k) K230217
Identifiers
- 510(k) Number
- K230217 FDA 510(k)
- FDA Product Code
- KGO FDA 510(k)
Classification
- Device Class
- Class I FDA 510(k)
- Legislation / Framework
- 21 CFR Part 878.4460 FDA 510(k)
- Regulation Number
- 878.4460 FDA 510(k)
- Advisory Committee
- General, Plastic Surgery FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Sterile Polyisoprene Powder Free Surgical Glove, Tested for Use with Chemothera… by Grand Work Plastic Products Co., Ltd. — Class I — FDA_510K — listed in FDA…
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 | K230217 | Class I | Active |
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Manufacturer
- Manufacturer
- Grand Work Plastic Products Co., Ltd.
Sources (1)
- FDA 510(k) K230217 24 fields · synced Jun 18, 2026