FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
PRE-MOISTENED CLEANSING PAD
K Number: K890514
·
Decision Apr 10, 1989
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
24
Applicant Total
92
Review Days
68
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Basic Information
- Device Name
- PRE-MOISTENED CLEANSING PAD
- K Number
- K890514
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Applicant
- Bausch & Lomb, Inc.
- Date Received
- February 1, 1989
- Decision Date
- April 10, 1989
- Product Code
- LKB
- Advisory Committee
- Unknown
- 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 |
|---|---|---|---|
| LKB | Pad, Alcohol, Device Disinfectant | FDA unclassified | Unknown |
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