← FDA Medical Device Classifications
Device, General Purpose, Hematology
LOQ · Class II — Moderate Risk (510(k) clearance required) · Immunology · 21 CFR 866.6010
Classification
- FDA Product Code
LOQ- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 866.6010
- Review panel
- HE
- Medical specialty
- Immunology
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- Y
Market data
- Cleared 510(k) submissions
- 1
- Registered establishments
- 3
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown