Atlas FDA

LEECO T4 QUANT DIAGNOSTICS TEST KIT

FDA 510(k) clearance K822399 · decided 1982-09-13

Clearance details

K-number
K822399
Device name
LEECO T4 QUANT DIAGNOSTICS TEST KIT
Applicant
Leeco Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1982-08-10
Decision date
1982-09-13
Days to decision
34 days
Clearance type
Traditional
Product code
CDX
Device class
2
Regulation number
862.1700
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Mchenry, IL, 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
ELECSYS T4 ASSAY (K961490)Boehringer Mannheim Corp.1996-06-13
ACTIVE THYROXINE RIA (K954312)Diagnostic Systems Laboratories, Inc.1995-10-07
DELFIA NEONATAL THYROXINE KIT (K943416)Wallac OY1995-03-10
AXSYM(TM) TOTAL T4 (K934384)Abbott Laboratories1994-06-21
TOTAL T4 FPIA REAGENT SET/CALIBRATOR #T-1039,T-116 (K932980)Sigma Diagnostics, Inc.1993-10-18
STRATUS(R) TOTAL THYROXINE(T4) FLUOR ENZYME IMMUNO (K933426)Baxter Diagnostics, Inc.1993-08-26
IQ TT4 ASSAY (K931295)Becton Dickinson Advanced Diagnostics1993-07-20
AUTOBEAD(TM) T4 ENZYME IMMUNOASSAY TEST KIT (K926563)Bio-Chem Laboratory Systems, Inc.1993-03-18
ABBOTT IMX T4 (K925110)Abbott Laboratories1993-01-26
ABBOTT TDX/TDXFLX TT4 (K925109)Abbott Laboratories1993-01-04
TECHNICON DAX SYSTEM THYROXINE (T4) METHOD (K922945)Heraeus Kulzer, Inc.1992-10-14
THYROXINE (T4) COATED TUBE RIA (K921935)Monobind1992-07-07

Recalls involving this device

No recalls on record reference this clearance.