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

FLEXSURE HP

K Number: K934863 · Decision May 18, 1994
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
90
Applicant Total
42
Review Days
218

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Basic Information

Device Name
FLEXSURE HP
K Number
K934863
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3110
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Smithkline Diagnostics, Inc.
Date Received
October 12, 1993
Decision Date
May 18, 1994
Product Code
LYR
Advisory Committee
Microbiology
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
LYR Helicobacter Pylori

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Other Clearances by Smithkline Diagnostics, Inc.

K Number Device Name
K961062 FLEXSURE OBT
K960183 FLEXSURE HP,CONTROLS FOR FLEXSUREHP,FLEXPACK HP(ABBOTT DIAGNOSTICS)ANDCONTROLS FOR FLEXPACK HP (ABBOTT DIAGNOSTICS)
K880499 HEMOCCULT SENSITIVE TEST
K875131 (SKD) CHOLESTEROL TEST KIT
K862849 HEMOCCULT WIPE TEST
K854723 SKD ELECTROCHEMICAL SYSTEM (ECS)
K852841 RAPID DIRECT STREP A LATEX AGGLUTINATION TEST
K821884 GASTROCCULT TM
K821674 SPINCHEM ACID PHOSPHATASE REAGENT
K821184 SPIN CHEM REAGENTS & STANDARDS
Search all 42 clearances from Smithkline Diagnostics, Inc. →