FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
Sterilization Package/Reel
K Number: K241565
·
Decision Feb 24, 2025
Classifications
1
FEI Numbers
203
Registration Numbers
203
Same Product Code
316
Applicant Total
1
Review Days
269
Basic Information
- Device Name
- Sterilization Package/Reel
- K Number
- K241565
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.6850
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Anqing Clean Dental Instrument Technology Co., Ltd.
- Date Received
- May 31, 2024
- Decision Date
- February 24, 2025
- Product Code
- FRG
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| FRG | Wrap, Sterilization | FDA class 2 | General Hospital |
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