Beurer IPL 5500 device/ IPL 5000/ IPL PureSkin Pro— 510(k) K181121
Substantially EquivalentHome Well Trading, Ltd.
FDA 510(k) clearance K181121 for Beurer IPL 5500 device/ IPL 5000/ IPL PureSkin Pro, Substantially Equivalent on 2018-06-28. Applicant: Home Well Trading, Ltd.. Device class: 2.
Clearance details
- Applicant
- Home Well Trading, Ltd.
- Product code
- Code OHT
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tortola, VG
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More clearances from Home Well Trading, Ltd.
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