← FDA Medical Device Classifications
Electrosurgical Vessel And/Or Tissue Sealer. With Built-In Generator.
PDG · Class II — Moderate Risk (510(k) clearance required) · General, Plastic Surgery · 21 CFR 878.4400
Classification
- FDA Product Code
PDG- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 878.4400
- Review panel
- SU
- Medical specialty
- General, Plastic Surgery
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- Y
Definition
Intended for any procedure where vessel ligation (cutting and sealing), soft tissue grasping and dissection are performed.
Market data
- Cleared 510(k) submissions
- 1
- Registered establishments
- 0
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown