← FDA Medical Device Classifications
Piezo-Electric Stimulator For Relief Of Mosquito Bite Itch
OSG · Class II — Moderate Risk (510(k) clearance required) · Neurology · 21 CFR 882.5894
Classification
- FDA Product Code
OSG- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 882.5894
- Review panel
- NE
- Medical specialty
- Neurology
- Submission type
- 4
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Definition
Relief / Reduction of Mosquito Bite Itch
Market data
- Cleared 510(k) submissions
- 2
- Registered establishments
- 6
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown