FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE
K Number: K930842
·
Decision May 3, 1994
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
148
Applicant Total
15
Review Days
440
Basic Information
- Device Name
- THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE
- K Number
- K930842
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.4150
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- GRIESHABER & CO.
- Date Received
- February 17, 1993
- Decision Date
- May 3, 1994
- 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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|---|---|---|---|
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