FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

TOBRAMYCIN REAGENT TEST KIT

K Number: K813391 · Decision Dec 18, 1981
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
24
Applicant Total
281
Review Days
15

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Basic Information

Device Name
TOBRAMYCIN REAGENT TEST KIT
K Number
K813391
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Beckman Instruments, Inc.
Date Received
December 3, 1981
Decision Date
December 18, 1981
Product Code
LKB
Advisory Committee
Unknown
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
LKB Pad, Alcohol, Device Disinfectant

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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. →