Atlas FDA

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.