FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
VICKS POWERSHOT DRY THROAT & MOUTH RELIEF
K Number: K091419
·
Decision Aug 28, 2009
Classifications
1
FEI Numbers
39
Registration Numbers
40
Same Product Code
49
Applicant Total
2
Review Days
107
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Basic Information
- Device Name
- VICKS POWERSHOT DRY THROAT & MOUTH RELIEF
- K Number
- K091419
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- The Procter & Gamble Co.
- Date Received
- May 13, 2009
- Decision Date
- August 28, 2009
- Product Code
- LFD
- 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 |
|---|---|---|---|
| LFD | Saliva, Artificial | FDA unclassified | Unknown |
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Other Clearances by The Procter & Gamble Co.
| K Number | Device Name | ||
|---|---|---|---|
| K110669 | TAMPAX C PLASTIC TAMPONS, UNSCENTED | Jun 2, 2011 | Substantially Equivalent |