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

FASTEC 901 AGGLUTINATION PATTERN READER

K Number: K895967 · Decision Oct 30, 1989
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
257
Applicant Total
15
Review Days
18

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Basic Information

Device Name
FASTEC 901 AGGLUTINATION PATTERN READER
K Number
K895967
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Schiff & Co.
Date Received
October 12, 1989
Decision Date
October 30, 1989
Product Code
JJQ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

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