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

CARESIDE GLOBULIN

K Number: K980055 · Decision Jan 28, 1998
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
9
Review Days
22

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Basic Information

Device Name
CARESIDE GLOBULIN
K Number
K980055
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1330
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Exigent Diagnostics, Inc.
Date Received
January 6, 1998
Decision Date
January 28, 1998
Product Code
JGE
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
JGE Turbidimetric Method, Globulin

Other Clearances by Exigent Diagnostics, Inc.

K Number Device Name
K982118 CARESIDE ANALYZER
K981899 CARESIDE HDL-CHOLESTEROL
K981183 CARESIDE GLUCOSE
K980043 CARESIDE CREATININE
K980056 CARESIDE ANALYZER
K980057 CARESIDE BUN
K980042 CARESIDE TOTAL PROTEIN
K980041 CARESIDE ALBUMIN