FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ASICO SOFTIP INJECTOR SYSTEM
K Number: K103495
·
Decision Jun 29, 2011
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
62
Applicant Total
2
Review Days
212
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Basic Information
- Device Name
- ASICO SOFTIP INJECTOR SYSTEM
- K Number
- K103495
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.4300
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Asico, LLC
- Date Received
- November 29, 2010
- Decision Date
- June 29, 2011
- Product Code
- MSS
- Advisory Committee
- Ophthalmic
- Review Advisory Committee
- OP
- Third Party
- Y
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MSS | Folders And Injectors, Intraocular Lens (Iol) | FDA class 1 | Ophthalmic |
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Other Clearances by Asico, LLC
| K Number | Device Name | ||
|---|---|---|---|
| K073010 | ROYALE AE 9036 LSP INJECTOR | Nov 7, 2007 | Substantially Equivalent |