SERVOTRONIC EC100 SYSTEM
FDA 510(k) clearance K972857 · decided 1998-01-16
Clearance details
- K-number
- K972857
- Device name
- SERVOTRONIC EC100 SYSTEM
- Applicant
- Medicon EG
- Decision
- Substantially Equivalent
- Date received
- 1997-08-01
- Decision date
- 1998-01-16
- Days to decision
- 168 days
- Clearance type
- Traditional
- Product code
- HBC
- Device class
- 2
- Regulation number
- 882.4360
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Washington, DC, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.