Atlas FDA

QUANTEX IGA

FDA 510(k) clearance K962200 · decided 1996-09-25

Clearance details

K-number
K962200
Device name
QUANTEX IGA
Applicant
Instrumentation Laboratory CO
Decision
Substantially Equivalent
Date received
1996-06-07
Decision date
1996-09-25
Days to decision
110 days
Clearance type
Traditional
Product code
CZP
Device class
2
Regulation number
866.5510
Medical specialty
Immunology
Advisory committee
Immunology
Location
Lexington, MA, US
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
Yumizen C1200 Immunoglobulin A, Yumizen C1200 Immunoglobulin G, Yumizen C1200 Immunoglobulin M (K193525)HORIBA ABX SAS2020-06-26
IMMAGE SYSTEMS LOW CONCENTRATION IMMUNOGLOBULIN A REAGENT (K060130)Beckman Coulter, Inc.2006-02-13
ROCHE DIAGNOSTICS TINA-QUANT IGA GEN.2 (K040435)Roche Diagnostics Corp.2004-03-10
N LATEX IGA (K024038)Dade Behring, Inc.2003-02-13
WAKO IGA II-HA, IMMUNOGLOBULIN CALIBRATOR SET, IMMUNOGLOBULIN STANDRAD (K993927)Wako Chemicals USA, Inc.2000-01-14
IGA (K983359)Abbott Laboratories1998-11-04
IGA IMMUNOTURBIDIMETRIC & CALIBRATOR (K955794)Randox Laboratories, Ltd.1996-04-05
BOEHRINGER MANNHEIM IGA ASSAY (K955907)Boehringer Mannheim Corp.1996-02-09
N LATEX IGA (K952309)Behring Diagnostics, Inc.1995-06-20
IGA SUBCLASS RID KIT FOR DIAGNOSTIC USE (K931806)The Binding Site, Ltd.1993-07-16
IL TEST IMMUNOGLOBULIN A (K920014)Instrumentation Laboratory CO1992-06-16
TITAN GEL IMMUNOFIX KIT, CAT. NO. 3046 (K900422)Helena Laboratories1990-02-27

Recalls involving this device

No recalls on record reference this clearance.