FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
TIDI FACEMASK
K Number: K092580
·
Decision Feb 23, 2010
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
606
Applicant Total
3
Review Days
186
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Basic Information
- Device Name
- TIDI FACEMASK
- K Number
- K092580
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4040
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Tidi Products,Llc
- Date Received
- August 21, 2009
- Decision Date
- February 23, 2010
- Product Code
- FXX
- Advisory Committee
- General, Plastic Surgery
- 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 |
|---|---|---|---|
| FXX | Mask, Surgical | FDA class 2 | General, Plastic Surgery |
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