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

ACCESS CK-MB ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 33300, 33305, 33309, 33306

K Number: K994439 · Decision Jan 14, 2000
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
47
Applicant Total
270
Review Days
22

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Basic Information

Device Name
ACCESS CK-MB ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 33300, 33305, 33309, 33306
K Number
K994439
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Beckman Coulter, Inc.
Date Received
December 23, 1999
Decision Date
January 14, 2000
Product Code
JHX
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
JHX Fluorometric Method, Cpk Or Isoenzymes

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