FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
BAUSCH & LOMB VERTOMETER V-5
K Number: K862518
·
Decision Aug 11, 1986
Classifications
1
FEI Numbers
64
Registration Numbers
65
Same Product Code
15
Applicant Total
92
Review Days
41
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Basic Information
- Device Name
- BAUSCH & LOMB VERTOMETER V-5
- K Number
- K862518
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.1425
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Applicant
- Bausch & Lomb, Inc.
- Date Received
- July 1, 1986
- Decision Date
- August 11, 1986
- Product Code
- HLM
- Advisory Committee
- Ophthalmic
- Review Advisory Committee
- OP
- 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 |
|---|---|---|---|
| HLM | Instrument, Measuring, Lens, Ac-Powered | FDA class 1 | Ophthalmic |
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