VERAPLUG
FDA 510(k) clearance K140352 · decided 2014-11-13
Clearance details
- K-number
- K140352
- Device name
- VERAPLUG
- Applicant
- Krishna Imports Inc Dba Stephens Instruments
- Decision
- Substantially Equivalent
- Date received
- 2014-02-12
- Decision date
- 2014-11-13
- Days to decision
- 274 days
- Clearance type
- Traditional
- Product code
- LZU
- Device class
- U
- Medical specialty
- Unknown
- Advisory committee
- Unknown
- Location
- Lexington, KY, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.