FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
PILL PHONE
K Number: K060298
·
Decision Mar 29, 2006
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
1
Applicant Total
1
Review Days
51
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Basic Information
- Device Name
- PILL PHONE
- K Number
- K060298
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.5050
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Vocel
- Date Received
- February 6, 2006
- Decision Date
- March 29, 2006
- Product Code
- NXQ
- Advisory Committee
- Physical Medicine
- 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 |
|---|---|---|---|
| NXQ | Reminder, Medication | FDA class 1 | Physical Medicine |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (NXQ), ordered by most recent decision date.
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