FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
FirstFit Surgical Kit
K Number: K240763
·
Decision Dec 18, 2024
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
39
Applicant Total
3
Review Days
273
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Basic Information
- Device Name
- FirstFit Surgical Kit
- K Number
- K240763
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 874.3730
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Freudenberg Medical, LLC
- Date Received
- March 20, 2024
- Decision Date
- December 18, 2024
- Product Code
- EWL
- Advisory Committee
- Ear, Nose, Throat
- Review Advisory Committee
- EN
- 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 |
|---|---|---|---|
| EWL | Prosthesis, Laryngeal (Taub) | FDA class 2 | Ear, Nose, Throat |
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