Atlas FDA

IDEIA(TM) CHLAMYDIA BLOCKING REAGENTS, MODIFICATION

FDA 510(k) clearance K940564 · decided 1996-01-11

Clearance details

K-number
K940564
Device name
IDEIA(TM) CHLAMYDIA BLOCKING REAGENTS, MODIFICATION
Applicant
Dako Diagnostics , Ltd.
Decision
Substantially Equivalent
Date received
1994-02-03
Decision date
1996-01-11
Days to decision
707 days
Clearance type
Traditional
Product code
LJC
Device class
1
Regulation number
866.3120
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Cambridgeshire, 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
CT OIA (K032330)Thermo Biostar, Inc.2004-03-02
IDEIA PCE CHLAMYDIA (K033865)Dakocytomation, Ltd.2004-01-21
CHLAMYDIA IGG ELISA TEST SYSTEM (K033079)Trinity Biotech USA2003-11-26
MODIFICATION OF SYVA MICROTRAK II CHLAMYDIA EIA (K982210)Dade Behring, Inc.1998-07-09
CHLAMYDIA IGG ELISA TEST SYSTEM (K962558)Armkel, LLC1997-02-24
ACCESS CHLAMYDIA ASSAY (K960850)Bio-Rad Laboratories, Inc.1997-02-04
VIDAS CHLAMYDIA BLOCKING ASSAY (K955627)Biomerieux Vitek, Inc.1996-10-07
IMX SELECT CHLAMYDIA (K936054)Abbott Laboratories1996-05-30
CHLAMYDIA OIA (K951010)Biostar, Inc.1995-10-07
QUICKVUE(R) CHLAMYDIA TEST (K946276)Quidel Corp.1995-05-19
ACCESS(R) CHLAMYDIA EIA AND BLOCKING ASSAY (K935807)Bio-Rad Laboratories, Inc.1995-05-19
CHLAMYDIA MICROPLATE EIA, CHLAMYDIA MICROPLAE EIA BLOCKING ASSAY (K935393)Bio-Rad Laboratories, Inc.1994-09-20

Recalls involving this device

No recalls on record reference this clearance.