← FDA Medical Device Classifications
Dilator, Esophageal
KNQ · Class II — Moderate Risk (510(k) clearance required) · Gastroenterology, Urology · 21 CFR 876.5365
Classification
- FDA Product Code
KNQ- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 876.5365
- Review panel
- GU
- Medical specialty
- Gastroenterology, Urology
- Submission type
- 4
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Market data
- Cleared 510(k) submissions
- 40
- Registered establishments
- 57
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown