← FDA Medical Device Classifications
Nebulizer (Direct Patient Interface)
CAF · Class II — Moderate Risk (510(k) clearance required) · Anesthesiology · 21 CFR 868.5630
Classification
- FDA Product Code
CAF- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 868.5630
- Review panel
- AN
- Medical specialty
- Anesthesiology
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Market data
- Cleared 510(k) submissions
- 507
- Registered establishments
- 190
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown