FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
IVALON OPHTHALMIC SPONGE
K Number: K946016
·
Decision Mar 22, 1995
Classifications
1
FEI Numbers
78
Registration Numbers
79
Same Product Code
46
Applicant Total
3
Review Days
103
Basic Information
- Device Name
- IVALON OPHTHALMIC SPONGE
- K Number
- K946016
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.4790
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- IVALON
- Date Received
- December 9, 1994
- Decision Date
- March 22, 1995
- Product Code
- HOZ
- 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 |
|---|---|---|---|
| HOZ | Sponge, Ophthalmic | FDA class 2 | Ophthalmic |
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