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

SAITRON 430 RANDOM ACCESS CHEMISTRY ANALYZER

K Number: K884035 · Decision Dec 29, 1988
Classifications
1
FEI Numbers
174
Registration Numbers
174
Same Product Code
207
Applicant Total
82
Review Days
97

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Basic Information

Device Name
SAITRON 430 RANDOM ACCESS CHEMISTRY ANALYZER
K Number
K884035
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2160
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Sclavo, Inc.
Date Received
September 23, 1988
Decision Date
December 29, 1988
Product Code
JJE
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
JJE Analyzer, Chemistry (Photometric, Discrete), For Clinical Use

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K Number Device Name
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K895822 TOTAL BILIRUBIN L.F.
K895847 CREATININE 340 (ENZYMATIC)
K880049 CHOLINESTERASE - BUTYRYTHIOCHOLINE SUBSTRATE
K880199 CHOLINESTERASE - ACETYTHIOCHOLINE SUBSTRATE
K873496 ATYPICAL CHOLINESTERASE
K884649 TOTAL IRON BINDING CAPACITY TEST
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