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

INFECTIOUS MONONUCLEOSIS (IM) CARD & LIQUID TEST

K Number: K880148 · Decision Feb 10, 1988
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
58
Applicant Total
15
Review Days
28

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Basic Information

Device Name
INFECTIOUS MONONUCLEOSIS (IM) CARD & LIQUID TEST
K Number
K880148
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5640
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Ampcor, Inc.
Date Received
January 13, 1988
Decision Date
February 10, 1988
Product Code
KTN
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
KTN System, Test, Infectious Mononucleosis

Similar 510(k) Clearances

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

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Other Clearances by Ampcor, Inc.

K Number Device Name
K922297 INFECTIOUS MONONUCLEOSIS QIK-DOT IM DRY CARD TEST
K922296 IMFECTIOUS MONONUCLEOSIS IM LIQUID CARD TEST
K910438 DIPSTICK SALMONELLA
K893873 SINGLE AND DUAL BAND DIPSTICK HCG TEST
K890048 QUIK-DOT TOXOPLASMOSIS
K892146 C REACTIVE PROTEIN LIQUID
K892119 QUIK-DOT C REACTIVE PROTEIN
K890025 QUIK-DOT ANTISTREPTOLYSIN-O
K884750 GROUP A STREP, BETA-STREP
K880163 PREGNANCY (HCG) CARD & LIQUID TEST
Search all 15 clearances from Ampcor, Inc. →