Atlas FDA

EMIT CAFFEINE ASSAY

FDA 510(k) clearance K853872 · decided 1986-06-13

Clearance details

K-number
K853872
Device name
EMIT CAFFEINE ASSAY
Applicant
Syva Co.
Decision
Substantially Equivalent
Date received
1985-09-17
Decision date
1986-06-13
Days to decision
269 days
Clearance type
Traditional
Product code
KLS
Device class
2
Regulation number
862.3880
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Palo Alto, CA, 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
VITROS CHEMISTRY PRODUCTS CAFFN REAGENT KIT AND TDM PERFORMANCE VERIFIERS I, II AND III (K042520)Ortho-Clinical Diagnostics, Inc.2004-11-30
EMIT CAFFEINE ASSAY (K042407)Dade Behring, Inc.2004-10-28
ROCHE ONLINE THEOPHYLLINE (K020740)Roche Diagnostics Corp.2002-04-16
RANDOX THEOPHYLLINE (K011771)Randox Laboratories, Ltd.2002-01-17
ACS: 180 AND ADVIA CENTAUR THEOPHYLLINE 2 ASSAY (K013272)Bayer Corp.2001-10-25
MODIFICATION TO EMIT 2000 THEOPHYLLINE ASSAY, MODEL OSR 4P229 (K011166)Syva Co., Dade Behring, Inc.2001-05-10
ABBOTT AEROSET THEOPHYLLINE ASSAY AND CALIBRATORS; MODELS 1E09 AND 6E89 (K993029)Syva Co.2000-01-27
ACE THEOPHYLLINE REAGENT, THEO CALIBRATORS (K973583)Schiapparelli Biosystems, Inc.1997-11-12
ACCUMETER THEOPHYLLINE TEST (K972495)Chemtrak, Inc.1997-10-10
CEDIA THEOPHYLLINE ASSAY (K961462)Boehringer Mannheim Corp.1996-06-27
IMMULITE THEOPHYLLINE (K954569)Diagnostic Products Corp.1995-11-13
THEOPHYLLINE ENZYME IMMUNOASSAY (K952596)Diagnostic Reagents, Inc.1995-08-11

Recalls involving this device

No recalls on record reference this clearance.