FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PHENYTOIN REAGENT TEST KIT

K Number: K802038 · Decision Oct 23, 1980
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
4
Applicant Total
281
Review Days
59

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Basic Information

Device Name
PHENYTOIN REAGENT TEST KIT
K Number
K802038
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3900
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Beckman Instruments, Inc.
Date Received
August 25, 1980
Decision Date
October 23, 1980
Product Code
DID
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DID Bacillus Subtilis Microbiology Assay, Tobramycin

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Other Clearances by Beckman Instruments, Inc.

K Number Device Name
K973448 ACCESS TOXOPLASMA IGM REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 34460, 34465, 34469
K982250 ACCESS FREE T4 REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER
K981403 IMMAGE IMMUNOCHEMISTRY SYSTEM VALPROIC ACID (VPA) REAGENT
K981354 ACCESS AFP REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER MODEL NUMBER 33211
K980173 ACCESS TOTAL BHCG REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER; 33500, 33505
K974816 ACCESS(R) PSA REAGENTS ON THE ACCESS(R) IMMUNOASSAY ANALYZER 33220, 33225, 33229
K974564 IMMAGE IMMUNOCHEMISTRY SYSTEM ALPHA-2-MACROGLOBULIN REAGENT
K974110 IMMAGE IMMUNOCHEMISTRY SYSTEM ANTITHROMBIN III (AT3) REAGENT
K974452 VIGIL LIPID CONTROL
K973932 BECKMAN CALIBRATOR 2 (CAL2)
Search all 281 clearances from Beckman Instruments, Inc. →