FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MICROSCIS(TM) INTROCULAR SCISSOR SYSTEM
K Number: K913837
·
Decision Nov 5, 1991
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
2
Review Days
71
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Basic Information
- Device Name
- MICROSCIS(TM) INTROCULAR SCISSOR SYSTEM
- K Number
- K913837
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.4150
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Vision Medical, Inc.
- Date Received
- August 26, 1991
- Decision Date
- November 5, 1991
- 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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Other Clearances by Vision Medical, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K913273 | DROLITE(TM) LIGHT SOURCE | Dec 4, 1991 | Substantially Equivalent |