ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORY
FDA 510(k) clearance K861372 · decided 1986-06-19
Clearance details
- K-number
- K861372
- Device name
- ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORY
- Applicant
- Snowden-Pencer
- Decision
- Substantially Equivalent
- Date received
- 1986-04-11
- Decision date
- 1986-06-19
- Days to decision
- 69 days
- Clearance type
- Traditional
- Product code
- GEI
- Device class
- 2
- Regulation number
- 878.4400
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Norcross, GA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.