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

3388 REPORTING INTEGRATOR

K Number: K792158 · Decision Nov 16, 1979
Classifications
1
FEI Numbers
115
Registration Numbers
116
Same Product Code
77
Applicant Total
230
Review Days
18

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Basic Information

Device Name
3388 REPORTING INTEGRATOR
K Number
K792158
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2100
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Hewlett-Packard Co.
Date Received
October 29, 1979
Decision Date
November 16, 1979
Product Code
JQP
Advisory Committee
Clinical Chemistry
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
JQP Calculator/Data Processing Module, For Clinical Use

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