FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
EZ SPLINT & EZ SPLINT PM
K Number: K022809
·
Decision Oct 17, 2003
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
70
Applicant Total
3
Review Days
420
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Basic Information
- Device Name
- EZ SPLINT & EZ SPLINT PM
- K Number
- K022809
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Power Products, Inc.-Splintek
- Date Received
- August 23, 2002
- Decision Date
- October 17, 2003
- 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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