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

LYPHOCHEK IMMUNOASSAY SERUM CONTROL LEVEL I,II,III

K Number: K864137 · Decision Nov 7, 1986
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
28
Applicant Total
319
Review Days
17

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Basic Information

Device Name
LYPHOCHEK IMMUNOASSAY SERUM CONTROL LEVEL I,II,III
K Number
K864137
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Bio-Rad
Date Received
October 21, 1986
Decision Date
November 7, 1986
Product Code
KIJ
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
KIJ Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment

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