← FDA Medical Device Classifications
Tomography, Optical Coherence
OBO · Class II — Moderate Risk (510(k) clearance required) · Ophthalmic · 21 CFR 886.1570
Classification
- FDA Product Code
OBO- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 886.1570
- Review panel
- OP
- Medical specialty
- Ophthalmic
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Definition
Viewing, imaging, measurement, and analysis of ocular structures. Diagnostic device to aid in the detection and management of various ocular diseases.
Market data
- Cleared 510(k) submissions
- 65
- Registered establishments
- 30
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown