FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
NEWGEL AND NEWGEL PLUS E
K Number: K041704
·
Decision Oct 17, 2005
Classifications
1
FEI Numbers
190
Registration Numbers
190
Same Product Code
80
Applicant Total
3
Review Days
481
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Basic Information
- Device Name
- NEWGEL AND NEWGEL PLUS E
- K Number
- K041704
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4025
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Newmedical Technology, Inc.
- Date Received
- June 23, 2004
- Decision Date
- October 17, 2005
- Product Code
- MDA
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| MDA | Elastomer, Silicone, For Scar Management | FDA class 1 | General, Plastic Surgery |
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