FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
INTRAOCULAR LENS GUIDE
K Number: K823222
·
Decision Dec 28, 1982
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
38
Applicant Total
17
Review Days
60
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Basic Information
- Device Name
- INTRAOCULAR LENS GUIDE
- K Number
- K823222
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.4300
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Applicant
- American Medical Optics
- Date Received
- October 29, 1982
- Decision Date
- December 28, 1982
- Product Code
- KYB
- 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 |
|---|---|---|---|
| KYB | Lens, Guide, Intraocular | FDA class 1 | Ophthalmic |
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Other Clearances by American Medical Optics
| K Number | Device Name | ||
|---|---|---|---|
| K860001 | BARRAQUER-KRUMEICH REFRACTIVE SET | Feb 4, 1986 | Substantially Equivalent |
| K851263 | AMER. MEDICAL OPTIC MONOCULAR DIRECT OPHTHALMASCOP | May 1, 1985 | Substantially Equivalent |
| K851264 | AMER. MEDICAL OPTICS MONOCULAR INDIRECT OPHTHALMAS | May 1, 1985 | Substantially Equivalent |
| K851262 | AMER. MEDICAL OPTICAL BINOCULAR INDIRECT OPHTHALMA | Apr 30, 1985 | Substantially Equivalent |
| K844150 | MEDICAL OPTICS PHACOEMULSIFICATION KIT | Dec 11, 1984 | Substantially Equivalent |
| K843966 | ARGON/KRYPTON LASER PHOTOCOAGULATOR SYS | Nov 8, 1984 | Substantially Equivalent |
| K843965 | ARGON LASER PHOTOCOAGULATOR SYS | Nov 6, 1984 | Substantially Equivalent |
| K842197 | AMERICAN MEDICAL OPTICS I/A KIT- IRRIG | Oct 1, 1984 | Substantially Equivalent |
| K842504 | AMER. MEDICAL OPTICS DIGITAL KERATO- | Oct 1, 1984 | Substantially Equivalent |
| K842127 | AMERICAN MEDICAL OPTICS IMAGING SYS | Sep 7, 1984 | Substantially Equivalent |