YA MEI FIRST AID KIT— 510(k) K031130
Substantially EquivalentYa Mei Technology Co., Ltd.
FDA 510(k) clearance K031130 for YA MEI FIRST AID KIT, Substantially Equivalent on 2003-06-27. Applicant: Ya Mei Technology Co., Ltd.. Device class: 1.
Clearance details
- Applicant
- Ya Mei Technology Co., Ltd.
- Product code
- Code KGO
- Device class
- Class 1
- Regulation
- 21 CFR 878.4460
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Littleton, CO, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.