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

ES 22

K Number: K854243 · Decision Nov 19, 1985
Classifications
1
FEI Numbers
180
Registration Numbers
180
Same Product Code
207
Applicant Total
340
Review Days
29

Basic Information

Device Name
ES 22
K Number
K854243
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2160
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
BOEHRINGER MANNHEIM CORP.
Date Received
October 21, 1985
Decision Date
November 19, 1985
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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