FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
VeriSplint
K Number: K190107
·
Decision Jul 10, 2019
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
70
Applicant Total
4
Review Days
169
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Basic Information
- Device Name
- VeriSplint
- K Number
- K190107
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Whip Mix Corporation
- Date Received
- January 22, 2019
- Decision Date
- July 10, 2019
- Product Code
- MQC
- Advisory Committee
- Unknown
- Review Advisory Committee
- DE
- 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 |
|---|---|---|---|
| MQC | Mouthguard, Prescription | FDA unclassified | Unknown |
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