FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
THROAT MOI-STIR
K Number: K840807
·
Decision May 25, 1984
Classifications
1
FEI Numbers
39
Registration Numbers
40
Same Product Code
49
Applicant Total
3
Review Days
91
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Basic Information
- Device Name
- THROAT MOI-STIR
- K Number
- K840807
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Applicant
- Kingswood Laboratories, Inc.
- Date Received
- February 24, 1984
- Decision Date
- May 25, 1984
- 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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