DUAL SWITCH
FDA 510(k) clearance K141908 · decided 2014-10-22
Clearance details
- K-number
- K141908
- Device name
- DUAL SWITCH
- Applicant
- Laser Engineering, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2014-07-15
- Decision date
- 2014-10-22
- Days to decision
- 99 days
- Clearance type
- Special
- Product code
- GEX
- Device class
- 2
- Regulation number
- 878.4810
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Nashville, TN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.