← Back to catalogue
Hk Liposuction Aspirator, Model Ap-Iii & Ap230-Iii
FDA 510(k)Class II (US FDA 510(k))
510(k) K032802
Identifiers
- 510(k) Number
- K032802 FDA 510(k)
- FDA Product Code
- QPB FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 878.5040 FDA 510(k)
- Regulation Number
- 878.5040 FDA 510(k)
- Advisory Committee
- General, Plastic Surgery FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Hk Liposuction Aspirator, Model Ap-Iii & Ap230-Iii by Hk Surgical Inc. — 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 | K032802 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Hk Surgical Inc.
- FDA Applicant
- Hk Surgical, Inc.
Sources (1)
- FDA 510(k) K032802 24 fields · synced Jun 18, 2026