FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

UC IMU B

K Number: K904137 · Decision Nov 21, 1990
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
42
Applicant Total
4
Review Days
76

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Basic Information

Device Name
UC IMU B
K Number
K904137
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5600
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Eucardio Laboratory, Inc.
Date Received
September 6, 1990
Decision Date
November 21, 1990
Product Code
DFC
Advisory Committee
Immunology
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
DFC Lipoprotein, Low-Density, Antigen, Antiserum, Control

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DFC), ordered by most recent decision date.

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Other Clearances by Eucardio Laboratory, Inc.

K Number Device Name
K942464 UC QIK 1-STEP HCG TEST
K926500 UC QIK PREGNANCY TEST
K904125 UC IMU A