← FDA Medical Device Classifications
Regulator, Vacuum
KDP · Class II — Moderate Risk (510(k) clearance required) · General Hospital · 21 CFR 880.6740
Classification
- FDA Product Code
KDP- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 880.6740
- Review panel
- HO
- Medical specialty
- General Hospital
- Submission type
- 4
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Market data
- Cleared 510(k) submissions
- 21
- Registered establishments
- 28
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown