FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BIOMEK 1000 AUTOMATED LABORATORY WORK STATION

K Number: K870544 · Decision Apr 22, 1987
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
139
Applicant Total
281
Review Days
72

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Basic Information

Device Name
BIOMEK 1000 AUTOMATED LABORATORY WORK STATION
K Number
K870544
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2750
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Beckman Instruments, Inc.
Date Received
February 9, 1987
Decision Date
April 22, 1987
Product Code
JQW
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
JQW Station, Pipetting And Diluting, For Clinical Use

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Other Clearances by Beckman Instruments, Inc.

K Number Device Name
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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. →