Atlas FDA

HEVYLITE HUMAN IGA KAPPA KIT FOR USE ON SIEMENS BNII, HEVYLITE HUMAN IGA LAMBDA KIT FOR USE ON SIEMENS BNII

FDA 510(k) clearance K140105 · decided 2014-03-18

Clearance details

K-number
K140105
Device name
HEVYLITE HUMAN IGA KAPPA KIT FOR USE ON SIEMENS BNII, HEVYLITE HUMAN IGA LAMBDA KIT FOR USE ON SIEMENS BNII
Applicant
The Binding Site
Decision
Substantially Equivalent
Date received
2014-01-15
Decision date
2014-03-18
Days to decision
62 days
Clearance type
Traditional
Product code
OPX
Device class
2
Regulation number
866.5510
Medical specialty
Immunology
Advisory committee
Immunology
Location
Birmingham, GB
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Optilite Hevylite IgA Kappa Kit, Optilite Hevylite IgA Lambda Kit (K160819)The Binding Site Group , Ltd.2016-06-16
Hevylite Human IgA Kappa Kit for use on SPAPLUS, Hevylite Human IgA Lambda Kit for use on SPAPLUS (K151759)The Binding Site Group , Ltd.2015-11-06

Recalls involving this device

No recalls on record reference this clearance.