← FDA Medical Device Classifications
Lens, Guide, Intraocular
KYB · Class I — Low Risk (general controls) · Ophthalmic · 21 CFR 886.4300
Classification
- FDA Product Code
KYB- Device class
- Class I — Low Risk (general controls)
- Regulation
- 21 CFR 886.4300
- Review panel
- OP
- Medical specialty
- Ophthalmic
- Submission type
- 4
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Market data
- Cleared 510(k) submissions
- 39
- Registered establishments
- 38
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown