E275
FDA 510(k) clearance K032653 · decided 2003-09-12
Clearance details
- K-number
- K032653
- Device name
- E275
- Applicant
- Micro Current Technology, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2003-08-28
- Decision date
- 2003-09-12
- Days to decision
- 15 days
- Clearance type
- Traditional
- Product code
- GZJ
- Device class
- 2
- Regulation number
- 882.5890
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Seattle, WA, US
- Third-party review
- Yes
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.