Atlas FDA

DSL ACTIVE T3 EIA

FDA 510(k) clearance K971270 · decided 1997-05-22

Clearance details

K-number
K971270
Device name
DSL ACTIVE T3 EIA
Applicant
Diagnostic Systems Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1997-04-04
Decision date
1997-05-22
Days to decision
48 days
Clearance type
Traditional
Product code
CDP
Device class
2
Regulation number
862.1710
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Webster, TX, 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
REPROBEAD T3 ENZYME IMMUNOASSAY REAGENT KIT (CATALOG# 104) (K001607)Repromedix Corp.2000-10-05
CHIRON DIAGNOSTICS ACS: 180 FT3 (K991692)Chiron Diagnostics Corp.1999-06-18
TOTAL T3 ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1005 (K991311)Biocheck, Inc.1999-06-02
AIA-PACK FT3 ASSAY (K991252)Tosoh Medics, Inc.1999-05-11
OPTICOAT T3 EIA KIT (K981824)Biotecx Laboratories, Inc.1998-12-22
ABBOTT ARCHITECT FREE T3 (K983439)Abbott Laboratories1998-11-20
ABBOTT ARCHITECT TOTAL T3 (K983434)Abbott Laboratories1998-11-20
AURAFLEX FT3 150 TEST PACK, AURAFLEX FT3 CALIBRATOR PACK (K974027)Alfa Biotech (Uk) , Ltd.1998-02-02
IMMULITE FREE T3 (K974634)Diagnostic Products Corp.1998-01-02
ACCESS TOTAL T3 REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER (K973966)Beckman Instruments, Inc.1997-10-31
TOTAL TRIIODOTHYRONINE(T3) MICROPLATE EIA (K971779)Monobind1997-06-16
NICHOLS ADVANTAGE CHEMILUMINESCENCE FREE T3 KIT (K965058)Nichols Institute Diagnostics1997-03-11

Recalls involving this device

No recalls on record reference this clearance.