FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ASPIRATION REVERSAL CONTROL (ARC) MODULE
K Number: K870068
·
Decision Feb 12, 1987
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
21
Review Days
35
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Basic Information
- Device Name
- ASPIRATION REVERSAL CONTROL (ARC) MODULE
- K Number
- K870068
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.4150
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Applicant
- Optical Micro Systems, Inc.
- Date Received
- January 8, 1987
- Decision Date
- February 12, 1987
- Product Code
- HQE
- 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 |
|---|---|---|---|
| HQE | Instrument, Vitreous Aspiration And Cutting, Ac-Powered | FDA class 2 | Ophthalmic |
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