Atlas FDA

Hevylite Human IgA Kappa Kit for use on SPAPLUS, Hevylite Human IgA Lambda Kit for use on SPAPLUS

FDA 510(k) clearance K151759 · decided 2015-11-06

Clearance details

K-number
K151759
Device name
Hevylite Human IgA Kappa Kit for use on SPAPLUS, Hevylite Human IgA Lambda Kit for use on SPAPLUS
Applicant
The Binding Site Group , Ltd.
Decision
Substantially Equivalent
Date received
2015-06-29
Decision date
2015-11-06
Days to decision
130 days
Clearance type
Traditional
Product code
OPX
Device class
2
Regulation number
866.5510
Medical specialty
Immunology
Advisory committee
Immunology
Location
Edgbaston, 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 SIEMENS BNII, HEVYLITE HUMAN IGA LAMBDA KIT FOR USE ON SIEMENS BNII (K140105)The Binding Site2014-03-18

Recalls involving this device

No recalls on record reference this clearance.