← FDA Medical Device Classifications
Needle, Fistula
FIE · Class II — Moderate Risk (510(k) clearance required) · Gastroenterology, Urology · 21 CFR 876.5540
Classification
- FDA Product Code
FIE- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 876.5540
- Review panel
- GU
- Medical specialty
- Gastroenterology, Urology
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Market data
- Cleared 510(k) submissions
- 79
- Registered establishments
- 17
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown